ClinicalTrials.gg
TerminatedNCT03311334Updated Apr 18, 2024Results posted

A Study of DSP-7888 Dosing Emulsion in Combination With Immune Checkpoint Inhibitors in Adult Patients With Advanced Solid Tumors

A Phase 1/2 interventional study of DSP-7888 Dosing Emulsion and Nivolumab in Renal Cell Carcinoma (RCC), Urothelial Carcinoma and Primary Peritoneal Cancer, sponsored by Sumitomo Pharma America, Inc.. Terminated at 19 sites in 2 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-04-18.

Sponsored by Sumitomo Pharma America, Inc. (part of Sumitomo Pharma Co., Ltd.) · Phase 1/2, Interventional, and Treatment

Why this study was terminated
Sponsor's decision to terminate development of the program.

Help build ClinicalTrials.gg — short surveys, remote interviews or testing, in your language. Take part →

Phase
Phase 1/2
Study type
Interventional
Enrollment
47
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-14

Among 1,142 studies in Carcinoma, Renal Cell with a site in United States — 156 open to participants now, 280 under way, 26 of them phase 3. Carcinoma, Renal Cell · United States.

Enrollment
449th of 1,008
47 · median 40
Started
2017
with 55 others
Phase 1/2
146 of 1,142
31 open now
Registered
704th of 1,142
by date

Among the 1,142 studies in Carcinoma, Renal Cell with a site in United States, this one is the 449th largest by enrollment of the 1,008 interventional ones that give a count, is one of 56 that started in 2017, is one of 146 in phase 1/2, and was the 704th registered.

Carcinoma, Renal Cell

2,038 studies on the registry are indexed under Carcinoma, Renal Cell; 395 are open to participants now.

Browse Carcinoma, Renal Cell studies →

Open to participants now

156 of the 1,142 studies in Carcinoma, Renal Cell with a site in United States are open now. Recruiting first, the newest first:

151 more — sign in →

All 156 open studies →

A study can be open while its sites in United States have not opened yet or have stopped. Only those recruiting at a site in United States →

Who these studies take

Of the 307 Carcinoma, Renal Cell studies recruiting now, 254 (83%) set no upper age limit and 18 (6%) stop at 75 or younger; 20 take children under 18; 19 take healthy volunteers.

This study: 18 Years and older · all sexes · no healthy volunteers.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

Was this useful?
Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 1,142 studies in Carcinoma, Renal Cell with a site in United States, or all of them as a file.
02

Study summary

This is a Phase 1b/2, open-label, multicenter study of DSP-7888 Dosing Emulsion in combination with checkpoint inhibitors (nivolumab or pembrolizumab) in adult patients with solid tumors, that consists of 2 parts: dose search part of the study (Phase 1b and Phase 1b Enrichment Cohort) and the dose expansion part of the study (Phase 2). In Phase 1b of this study there will be 2 arms: Arm 1 and Arm 2. In Arm 1, there will be 6 to 12 patients who will be dosed with DSP-7888 Dosing Emulsion and nivolumab and in Arm 2 there will be 6 to 12 patients who will be dosed with DSP-7888 Dosing Emulsion and pembrolizumab. In addition, an enrichment cohort of a further 10 patients who have locally advanced or metastatic Renal Cell Carcinoma or Urothelial Cancer with primary or acquired resistance to previous checkpoint inhibitors will be enrolled into Phase 1b of the study to help evaluate the preliminary antitumor activity of DSP-7888 Dosing Emulsion at the safe dose level identified in the dose-search part of the study, and will be dosed with DSP-7888 Dosing Emulsion and nivolumab, or DSP-7888 Dosing Emulsion and pembrolizumab, as per the investigator's preference. At the safe, recommended dose determined in Phase 1b, platinum-resistant ovarian cancer (PROC) patients will be enrolled in Phase 2 of the study with DSP-7888 Dosing Emulsion, exploring the combination with pembrolizumab (Arm 2). In Phase 2, approximately 40 patients with PROC will be initially enrolled; additional patients may be enrolled to further assess anti-tumor activities, but the total sample size will not exceed 60 patients. This brings the total maximum study population to approximately 84 patients.

03

Conditions studied

  • Renal Cell Carcinoma (RCC)
  • Urothelial Carcinoma
  • Primary Peritoneal Cancer
  • Platinum-resistant Ovarian Cancer (PROC)
  • Serous Epithelial Ovarian Cancer
  • Fallopian Tube Cancer

Keywords

  • DSP-7888
  • Nelatimotide
  • Adegramotide
  • immune checkpoint inhibitor
  • cancer vaccine
  • WT1
  • ICI
  • Wilms Tumor 1
  • Ombipepimut-S
  • nivolumab
  • Opdivo
  • pembrolizumab
  • Keytruda
  • Ovarian cancer
  • Platinum-resistant ovarian cancer
  • PROC
  • Serous epithelial ovarian cancer
  • High-grade serous epithelial ovarian cancer
  • HGSOC
  • Fallopian tube cancer
  • FTC
  • Peritoneal cancer
  • Primary peritoneal cancer
  • PPC
  • Renal cell carcinoma
  • Kidney cancer
  • RCC
  • Metastatic Renal Cell Carcinoma
  • Metastatic RCC
  • Metastatic kidney cancer
  • Advanced Renal Cell Carcinoma
  • Advanced RCC
  • Advanced kidney cancer
  • Urothelial carcinoma
  • Bladder cancer
  • Transitional cell carcinoma
  • UC
  • Metastatic urothelial carcinoma
  • Metastatic transitional cell carcinoma
  • Metastatic UC
  • Advanced urothelial carcinoma
  • Advanced UC
  • Advanced transitional cell carcinoma
04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria Phase 1b:

Patients must fulfill each of the following requirements:

  1. Phase 1b Dose Search Part Only: A or cytologically confirmed cancer that is and is approved to be treated with nivolumab or pembrolizumab with the following origins:

    • Nivolumab: unresectable or metastatic melanoma, metastatic NSCLC, advanced RCC, recurrent or metastatic squamous cell carcinoma of the head and neck, locally advanced or metastatic urothelial carcinoma, hepatocellular carcinoma, MSI-H/dMMR colorectal cancer
    • Pembrolizumab: unresectable or metastatic melanoma, metastatic NSCLC, recurrent or metastatic squamous cell carcinoma of the head and neck, locally advanced or metastatic urothelial carcinoma, unresectable or metastatic MSI-H/dMMR solid tumors, recurrent locally advanced or metastatic gastric cancer or gastroesophageal junction adenocarcinoma, recurrent or metastatic cervical cancer

    In addition, the following requirements must be fulfilled:

    1. Patients must not be considered eligible for a potentially curative resection.
    2. Patients who are eligible for therapy based on either criterion (i) or (ii) below:

    (i) Patients progressed on their prior treatment before initiating treatment on current study, OR (ii) Patients who are currently being treated with nivolumab or pembrolizumab and have achieved at least stable disease (SD), and who, in the judgment of their treating physicians, could benefit from the addition of DSP-7888 Dosing Emulsion vaccine to improve or maintain their response.

    Phase 1b Enrichment Cohort Only: Patients with locally advanced or metastatic RCC or urothelial carcinoma who have experienced disease progression per (iCPD) during or within 3 months of last dose of the most recent prior anti-PD-1/ PD-L1-based treatment

  2. Patients must be positive for at least 1 of the following human leukocyte antigens:

    1. HLA-A*02:01
    2. HLA-A*02:06
    3. HLA-A*24:02
    4. HLA-A*03:01
    5. HLA-B*15:01
  3. ≥ 18 years of age
  4. (ECOG) performance status of 0 or 1
  5. Patients must be able to provide with sufficient tumor tissue, or patients must consent to undergo tumor biopsy to acquire sufficient tissue before first administration of study
  6. Females of must have a negative serum pregnancy test
  7. Male or female patients of child-producing potential must agree to use or use prevention of pregnancy measures (true abstinence) during the study and for 6 months (for females and males alike) after the last dose
  8. Total of ≤ 2.0 mg/dL (≤ 3.0 mg/dL for patients with known Gilbert's syndrome)
  9. (AST) ≤ 3.0 × the (ULN) or \< 5 × ULN if considered to be due to liver metastases
  10. Alanine transaminase (ALT) ≤ 3.0 × the upper limit of normal (ULN) or \< 5 × ULN if considered to be due to liver metastases
  11. > 40 mL/min
  12. Multigated acquisition () scan or echocardiogram with left ventricular ejection fraction (LVEF) > 40%
  13. ≥ 3 months
  14. Patients must be willing to provide a signed and dated ICF

Exclusion Criteria Phase 1b:

Patients with any of the following will be excluded from the study:

  1. Anticancer chemotherapy (including molecular targeted drugs), immunotherapy, radiotherapy, or agents within 4 weeks of the first dose of DSP 7888 Dosing Emulsion
  2. Major surgery within 4 weeks prior to study treatment
  3. Patients who have received a within 4 weeks prior to the first dose
  4. Any known, untreated ; patients with treated brain metastases must be clinically stable for 4 weeks after completion of treatment for brain metastases and have radiographic image documentation of stability. Patients must have no clinical symptoms from brain metastases and not have required systemic > 10 mg/day prednisone or equivalent for at least 2 weeks prior to the first dose of study drug
  5. Patients who have multifocal glioblastoma
  6. Pregnant or breastfeeding
  7. Patients who have an active disease requiring > 10 mg/day prednisone or equivalent a. Patients with controlled hyperthyroidism must be negative for thyroglobulin and thyroid peroxidase antibodies and thyroid stimulating immunoglobulin prior to study drug administration
  8. Patients who have interstitial lung disease or active, non-infectious pneumonitis
  9. Known to a component of protocol therapy:

    1. Patients with known hypersensitivity to any of the components of DSP-7888 Dosing Emulsion.
    2. Patients with known hypersensitivity to nivolumab or pembrolizumab are excluded from receiving combination therapy that includes the agent to which they are hypersensitive
  10. Uncontrolled concurrent illness including, but not limited to: ongoing or active, uncontrolled bacterial, viral, or fungal infections requiring systemic therapy; non-healing or healing wounds; symptomatic congestive heart failure; unstable angina pectoris; severe and/or uncontrolled cardiac arrhythmia; significant pulmonary disease; or, psychiatric illness/social situations that would limit compliance with study requirements
  11. Patients with a history of another primary cancer with the exception of: (a) curatively resected non-melanoma skin cancer; (b) curatively treated cervical carcinoma in situ; (c) localized prostate cancer not requiring systemic therapy; and d) any another cancer from which the patient has been disease free for ≥ 2 years that, in the opinion of the Investigator and medical monitor for the Sponsor, will not affect patient outcome in the setting of the current diagnosis
  12. Patients who have a (QT corrected based on Fridericia's equation) interval > 480 msec ( = Grade 2) or other factors that increase the risk of QT prolongation or arrhythmic events (e.g. heart failure, hypokalemia, family history of long QT interval syndrome) at screening
  13. Patients who have a medical history of frequent or sustained ventricular ectopy
  14. Patients who have, in the opinion of the treating Investigator, any concurrent conditions that could pose an undue medical hazard or interfere with the interpretation of the study results
  15. Known history of (HIV) infection, active , or untreated
  16. Patients who have baseline signs and symptoms consistent with clinically significant, decreased pulmonary function: (1) blood saturation oxygen level (SpO2) \< 90% at rest on room air; (2) dyspnea at rest or required supplemental oxygen within 2 weeks of study enrollment

Inclusion Criteria Phase 2:

Patients eligible for inclusion must meet all of the following criteria:

  1. Patients must be female ≥ 18 years of age, able to understand study procedures, and subsequently agreed to participate in the study by providing a written obtained prior to any prescreening and screening procedures that are not standard of care 2.

Patients must be positive for at least 1 of the following human leukocyte antigens (HLA):

a. HLA-A*02:01 b. HLA-A*02:06 c. HLA-A*24:02 d. HLA-A*03:01 e. HLA-B*15:01

  1. Patients must have histologically diagnosed ovarian, fallopian tube, or primary peritoneal cancer with predominantly high-grade (Grade 2 or 3) serous epithelial features 4. Patients must be considered platinum resistant to last administered platinum-based therapy, defined as patient within 6 months after last dose of platinum-based therapy 5. Patients must have completed at least 1 but no more than 4 for serous epithelial ovarian, fallopian tube, or primary peritoneal cancer;
  1. Maintenance is not considered a separate line of treatment (even if patients with BRCA mutation positive received PARP-inhibitor following induction therapy with a platinum doublet including bevacizumab, etc.)
  2. and adjuvant systemic therapy will be counted as one line of therapy
  3. Patients must have received at least one platinum-based therapy

    1. Patients must have progression disease after last therapy and have according to (v1.1).
    1. Patients must have an ECOG performance status of 0 or 1. 8. Patients must have adequate organ function, defined as follows:

Hematological:

  1. (ANC) ≥ 1,500/μL (without granulocyte-colony stimulating factor (G-CSF))
  2. ≥ 100,000/μL (without transfusion)
  3. ≥ 9.0 g/dL (without transfusion)

Renal:

a. Serum Creatinine OR estimated glomerular filtration rate using the equation ≤ 1.5 × the upper limit of normal (ULN) OR 40 mL/min using the Cockcroft-Gault equation for patients with creatinine levels > 1.5 × ULN

Hepatic:

  1. Serum total bilirubin ≤ 1.5 ULN
  2. Aspartate aminotransferase (AST) and alanine transaminase (ALT) ≤ 2.5 × ULN OR ≤ 5 × ULN for patients with liver metastases

Cardiac:

  1. Multigated acquisition (MUGA) scan or echocardiogram with left ventricular ejection fraction (LVEF) ≥ 40%.
  2. QTcF (QT corrected based on Fridericia's equation) interval \< 480 msec

Coagulation:

  1. (INR) or Prothrombin Time (PT) ≤ 1.5 × ULN
  2. Activated Partial Thromboplastin Time (aPTT) or Partial Thromboplastin Time (PTT) ≤ 1.5 × ULN

    1. Patients must provide a fresh tissue biopsy, if medically feasible, or archival tissue as either a formalin-fixed and paraffin embedded FFPE) block or newly sectioned tissue on charged slides (equivalent to approximately 8-23 slides sectioned at 4-5μm thickness) 10. Patients of childbearing potential must have a negative serum or urine pregnancy test at screening 11. Patients must be either , free from menses > 12 months, surgically sterilized, or willing to use adequate contraception to prevent pregnancy or must agree to abstain from heterosexual activity throughout the study, starting with enrollment through 6 months after the last dose of study treatment 12. Life expectancy ≥ 3 months 13. Patients who had stayed on the last treatment for at least 12 weeks without any evidence of progression

Exclusion Criteria Phase 2:

Patients with any of the following will be excluded from the study:

  1. Primary platinum refractory patients defined as patients who experienced disease progression during the treatment with first-line platinum therapy
  2. Patients with a known, untreated brain metastasis. Patients with treated brain metastases must be clinically stable for 4 weeks after completion of treatment for brain metastases and have radiographic image documentation of stability. Patients must have no clinical symptoms from brain metastases and not have required systemic corticosteroids > 10 mg/day prednisone or equivalent for at least 4 weeks prior to the first dose
  3. Patients who have received prior treatment with any other anti-PD-1, or PD-L1 or PD-L2 agent or an antibody or a small molecule targeting other immuno-regulatory receptors or mechanisms (examples of such drugs include but are not limited to antibodies against CTLA-4, LAG-3, IDO, PD-L1, IL-2R, GITR)
  4. Patients who have received prior treatment with any other Wilms Tumor 1 (WT1)-related agents including peptide vaccine, dendric cell vaccine, and gene therapy
  5. Patients who have received treatment for ovarian cancer within the following time frame prior to the first dose of the study

    1. Cytotoxic chemotherapy, hormonal therapy; ≤ 3 weeks
    2. Targeted therapy except for monoclonal antibody; ≤ 3 weeks
    3. Immune therapy, biologic therapy (e.g. antibodies); ≤ 4 weeks
    4. Other investigational agents: ≤ 4 weeks
    5. Radiation therapy (except for localized radiotherapy for analgesic purpose) ≤ 4 weeks
    6. Radiation therapy (localized radiotherapy for analgesic purpose) ≤ 1 week
    7. Major surgery regardless of reason ≤ 4 weeks.
  6. Patients who have received a live vaccine within 4 weeks prior to the first dose.
  7. Any known additional that is progressing or requires active treatment with the exception of:

    1. curatively treated basal cell or squamous cell carcinoma of skin
    2. curatively treated superficial bladder cancer, carcinoma in situ of the cervix,
    3. any another cancer from which the patient has been disease free for ≥ 3 years without any active treatment that, in the opinion of the Investigator and medical monitor for the Sponsor, will not affect patient's outcome in the setting of the current diagnosis.
  8. Patients who have not recovered to \< CTCAE Grade 2 or baseline from toxic effect (with exception of alopecia and/or neuropathy) of prior cancer therapy.
  9. Patients who have an active autoimmune disease requiring systemic immunosuppression in excess of physiologic maintenance dose of corticosteroids (> 10 mg/day prednisone or equivalent) or any other forms of immunosuppressive therapy within 7 days prior to the first dose of study drug.
  10. Positive serology for HIV infection, active hepatitis B, or hepatitis C
  11. Patients who have a known history of bacillus tuberculosis (TB).
  12. Patients with impaired cardiac function or clinically significant cardiac disease;

    • New York Hospital Association Class III or IV cardiac disease, including preexisting clinically significant ventricular arrythmia, congestive heart failure, or cardiomyopathy
    • Unstable angina pectoris ≤ 6 months before study participation
    • Myocardial infarction or stroke ≤ 6 months before study participation
  13. Patients who have an interstitial lung disease or a history of pneumonitis that required oral or intravenous glucocorticoids to assist with management
  14. Patients with active, uncontrolled bacterial, viral, or fungal infections, requiring systemic therapy
  15. Patients with any psychiatric condition, substance abuse disorder, or social situation that would interfere with a patient's cooperation with the study requirements and schedule
  16. Patients with any condition that would, in the investigator's judgment, interfere with full participation including administration of study drugs, attending required visits or interfere with interpretation of study data
  17. Patients who are pregnant or breastfeeding
  18. Patients who have known hypersensitivity to DSP-7888 Dosing Emulsion, pembrolizumab, their components, or their
  19. Patient has dyspnea at rest (CTCAE ≥ Grade 3) or has required supplemental oxygen within 2 weeks of study enrollment
  20. Patients with history of bowel obstruction related to underlying disease within 3 months prior to the first dose of study treatment
Terms in these criteria, in plain language(41)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Histologically or cytologically confirmed

The diagnosis was confirmed by looking at a sample under a microscope: tissue from a biopsy or surgery (histology), or cells from a fluid or needle sample (cytology).

Your pathology report is the document that shows this.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

PD-1, PD-L1 and checkpoint inhibitors

PD-1, PD-L1 and CTLA-4 are proteins that act as brakes on the immune system. Checkpoint inhibitors, such as pembrolizumab or nivolumab, block them so the immune system can attack a cancer.

PD-L1 can also be measured in a tumour sample. Some scores count stained tumour cells only (TPS); others also count certain immune cells (CPS). The study names the score and the minimum it uses.

iRECIST and mRECIST

Versions of RECIST adapted to particular cases. iRECIST is for immunotherapy, where a tumour can look bigger for a while before it shrinks, so growth has to be confirmed on a later scan. mRECIST usually means the version for liver cancer (hepatocellular carcinoma), which measures only the part of a tumour that still has a blood supply.

ECOG performance status

A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.

Biopsy and archival tissue

A biopsy takes a small piece of tissue to examine. “Archival tissue” is a sample already taken, for example at diagnosis, and kept by the hospital.

Whether a stored sample will do depends on when it was taken, how much there is and what the study needs. Ask whether the study accepts your stored sample or needs a new biopsy.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

LVEF (left ventricular ejection fraction)

The share of blood the heart’s main pumping chamber (the left ventricle) pushes out with each beat, measured by an echocardiogram (heart ultrasound) or a MUGA scan. About 50–70% is normal.

Life expectancy

The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

Live vaccines

Vaccines made with a weakened form of the germ, such as measles–mumps–rubella (MMR), chickenpox and yellow fever. They can be risky when the immune system is weakened. Flu injections are not live; the nasal flu spray is.

Brain metastases

Cancer deposits in the brain from a cancer that started elsewhere in the body (CNS metastases include the spinal cord).

Studies differ: some leave out any brain metastases, some accept ones treated and stable for some weeks. Check what this study allows.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

QT and QTc

On an ECG, the QT interval is the time the heart’s lower chambers take to activate electrically and recover in each beat. QTc is that time adjusted for heart rate (QTcF by Fridericia’s formula, QTcB by Bazett’s). Some medicines lengthen it, and a long QTc can raise the risk of a dangerous heart rhythm.

The study may name a correction formula and a limit in milliseconds, often around 450–480.

CTCAE grade

The US National Cancer Institute’s scale of how severe an adverse event is — any unwanted medical event during a study, such as a symptom, an illness or an abnormal test result, whether or not a treatment caused it. Whether it did is judged separately.

1
Mild.
2
Moderate.
3
Severe.
4
Life-threatening.
5
Death due to the event.

“Side effects of earlier treatment resolved to grade 1 or less” means they have settled to mild or gone.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Relapsed and refractory

Relapsed: the illness came back after treatment had worked. Refractory: it did not respond to treatment, or stopped responding while still on it.

Line of therapy

A line of therapy is one course of treatment, which may combine several drugs. First-line is the first course given; second-line follows when that stops working or is not tolerated.

“Two prior lines” means two courses that count separately under the study’s rules — not simply two drugs. Ask the study team if you are unsure how yours are counted.

Adjuvant and neoadjuvant

Neoadjuvant treatment is given before the main treatment (usually surgery), often to shrink a tumour. Adjuvant treatment is given after it, to lower the chance of the cancer coming back.

Measurable disease

The amount of disease can be tracked with a defined measurement, so the study can see whether it shrinks or grows. It might be a tumour measured on a scan or, in some blood cancers such as myeloma, a marker measured in blood or urine.

The criteria or the study team say which measurement counts — having no tumour visible on a scan does not by itself rule you out.

RECIST

The standard rules for measuring tumours on CT or MRI scans, to tell whether a cancer is shrinking, stable or growing during treatment.

“Measurable disease per RECIST 1.1” usually means at least one tumour 10 mm or more at its longest on a CT scan, or a lymph node 15 mm or more across its short axis.

Absolute neutrophil count (ANC)

The number of neutrophils, white blood cells that help fight infection, in a given amount of blood. Too few raises the risk of infection.

It is a count, not a percentage of the white cells. Limits are written in units that mean the same: ≥ 1.5 × 10⁹/L is ≥ 1,500 per mm³ (µL). Each lab has its own reference range.

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

Creatinine clearance (CrCl)

How quickly the kidneys clear creatinine, a waste product, from the blood. A study may estimate it from a blood test with age, weight and sex (often by the Cockcroft–Gault formula), or measure it using blood and urine collected over a set time. Given in mL/min; higher is better.

INR, PT and aPTT (clotting tests)

Blood tests of how long blood takes to clot. The INR is the prothrombin time (PT) put on a common scale; about 1 is usual for someone not taking a blood thinner.

Criteria often make an exception for people on a blood thinner such as warfarin, whose INR is raised on purpose.

Postmenopausal

Periods have stopped for good: usually no period for 12 months in a row without another medical reason, sometimes confirmed by a blood test (FSH).

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Excipients

The other ingredients in a medicine besides the active drug, such as fillers, colours or preservatives.

05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
47 participants (actual)

Study arms

  • Experimental
    DSP-7888 Dosing Emulsion in combination with Nivolumab

    Drug: DSP-7888 Dosing Emulsion · Drug: Nivolumab

  • Experimental
    DSP-7888 Dosing Emulsion in combination with Pembrolizumab

    Drug: DSP-7888 Dosing Emulsion · Drug: Pembrolizumab

Interventions

  • DSP-7888 Dosing Emulsion will be administered intradermally (ID) every 7 days until cycle 3, and then every 14 days for combination with Nivolumab arm or every 21 days for combination with Pembrolizumab arm.

    Also known as: Ombipepimut-S (adegramotide and nelatimotide)

  • Nivolumab will be administered in the approved dose and schedule starting on Day 29 of the study.

    Also known as: Opdivo

  • Pembrolizumab will be administered in the approved dose and schedule starting on Day 22 of the study.

    Also known as: Keytruda

06

What researchers measure

Primary outcomes

  1. Number of Patients With Adverse Events and Serious Adverse Events

    Time frame: From the date of signing informed consent until 30 days after last dose for an average of 3 months.

  2. Determination of the Recommended Phase 2 Dose (RP2D) by Assessing Dose-limiting Toxicities (DLTs).

    The RP2D was based on the data collected during phase 1b.

    Time frame: 28 days

  3. Phase II: The Objective Response Rate (ORR) of DSP-7888 Dosing Emulsion Administered With Pembrolizumab in Patients With Platinum-resistant Ovarian Cancer (PROC).

    Defined as the proportion of patients who have achieved confirmed Complete Response or Partial Response by RECIST v1.1 based on investigator assessment.

    Time frame: Radiographic imaging every 6 weeks for 24 weeks and then every 12 weeks until progression for an average of 12 months

Secondary outcomes

  1. Phase Ib: The Objective Response Rate (ORR) of DSP-7888 Dosing Emulsion Administered With Pembrolizumab or Nivolumab

    Defined as the proportion of patients who have achieved confirmed complete response (CR) or partial response (PR) evaluated using RECIST v1.1 and iRECIST.

    Time frame: At 4 weeks for the nivolumab arm and at 6 weeks for the pembrolizumab arm and then at Weeks 12, 18, and 24 after the first dose of the DSP-7888 dosing emulsion

  2. Phase Ib: The Disease Control Rate (DCR) of DSP-7888 Dosing Emulsion Administered With Pembrolizumab or Nivolumab

    Defined as the percentage of patients who have achieved best overall response (BOR) of complete response (CR), partial response (PR), or stable disease (SD) per RECIST v1.1 and iRECIST.

    Time frame: At 4 weeks for the nivolumab arm and at 6 weeks for the pembrolizumab arm and then at Weeks 12, 18, and 24 after the first dose of the DSP-7888 dosing emulsion

  3. Phase Ib: Assessment of the Duration of Response (DOR) of Ombipepimut-S in Combination With Nivolumab or Pembrolizumab

    DOR is defined as the time from first documentation of response until the time of first documentation of disease progression by RECIST v1.1 and iRECIST or death by any cause.

    Time frame: At week 4 for patients on the nivolumab arm and week 6 for patients on the pembrolizumab arm. Thereafter weeks 12, 18 and 24 and every 12 weeks until progression or death.

  4. Phase Ib: Progression-free Survival (PFS) of DSP-7888 Dosing Emulsion Administered With Pembrolizumab or Nivolumab

    The percentage of participants with a complete response or partial response who have measurable disease at baseline imaging.

    Time frame: Radiographic imaging every 6 weeks for 24 weeks and then every 12 weeks until progression for an average of 12 months

  5. Phase Ib: The 6-month Progression-free Survival (PFS) Rate of Ombipepimut-S in Combination With Nivolumab or Pembrolizumab

    Defined as the proportion of patients who neither progressed by RECIST (v.1.1) nor died before 6 months (24 weeks) from the first study treatment

    Time frame: 6 months

  6. Phase Ib: Percentage of Patients With Overall Survival (OS) When Treated With Ombipepimut-S in Combination With Nivolumab or Pembrolizumab

    Time frame: 12 months

  7. Phase II: Assessment of the Duration of Response (DOR) of Ombipepimut-S in Combination With Pembrolizumab

    Defined as the time from the first documentation of a response (CR or PR) until time of first documentation of disease progression by RECIST v1.1 or death by any cause.

    Time frame: Radiographic imaging every 6 weeks for 24 weeks and then every 12 weeks until progression up to 24 months.

  8. Phase II: Disease Control Rate of Ombipepimut-S in Combination With Pembrolizumab

    Defined as the percentage of patients who have achieved best overall response (BOR) of complete response, partial response, or stable disease per RECIST (v.1.1)

    Time frame: Radiographic imaging every 6 weeks for 24 weeks and then every 12 weeks until progression, up to 24 months.

  9. Phase II: Assessment of the Progression-free Survival (PFS) of Ombipepimut-S in Combination With Pembrolizumab

    Defined as the time from the date of the first dose of study treatment to the earlier date of assessment of progression by RECIST v.1.1, or death by any cause

    Time frame: Radiographic imaging every 6 weeks for 24 weeks and then every 12 weeks until progression, up to 24 months

  10. Phase II: 6-month Progression-free Survival (PFS) of Ombipepimut-S in Combination With Pembrolizumab

    PFS is defined as the time from the date of the first dose of study treatment to the earlier date of assessment of progression by RECIST (v.1.1), or death by any cause

    Time frame: 6 months

  11. Phase II: Overall Survival of Patients Treated With Ombipepimut-S in Combination With Pembrolizumab

    Defined as the time from the date of first dose of study treatment to the date of death by any cause

    Time frame: Every 3 months from last dose of study treatment up to 24 months.

  12. Phase II: Immune Objective Response Rate (iORR) of Ombipepimut-S in Combination With Pembrolizumab

    Defined as the percentage of patients who have achieved confirmed immune complete response (iCR) or immune partial response (iPR), evaluated using iRECIST based on investigator's assessment.

    Time frame: Up to 24 months

  13. Phase II: Immune Disease Control Rate (iDCR) of Ombipepimut-S in Combination With Pembrolizumab

    Defined as the percentage of patients who have achieved best overall response of iCR, iPR, or immune stable disease (iSD), per iRECIST

    Time frame: Up to 24 months

  14. Phase II: Immune Progression-free Survival (iPFS) of Ombipepimut-S in Combination With Pembrolizumab

    Defined as the time from the date of the first dose of study treatment to the earlier date of assessment of progression by iRECIST or death by any cause

    Time frame: Up to 24 months

  15. Phase II: Immune Duration of Response (iDOR) of Ombipepimut-S in Combination With Pembrolizumab

    Defined as the time from the first documentation of response (iCR or iPR) until time of first documentation of disease progression by iRECIST, or death by any cause

    Time frame: Up to 24 months

  16. Phase II: Evaluation of the Safety and Tolerability of Ombipepimut-S in Combination With Pembrolizumab

    Demonstrated by the number of participants with adverse events and serious adverse events

    Time frame: Up to 24 months

07

Results

Posted Apr 18, 2024

Participant flow

Participant flow — Overall Study
MilestonePhase 1b - DSP-7888 10.5 mg + Nivolumab 240 mgPhase 1b - DSP-7888 10.5 mg + Pembrolizumab 200 mg/8mLPhase 2 - DSP-7888 10.5mg + Pembrolizumab 200mg/8mL
Started7931
Completed7931
Not completed000

Outcome measures

PrimaryNumber of Patients With Adverse Events and Serious Adverse Events
Time frame:
From the date of signing informed consent until 30 days after last dose for an average of 3 months.
Reported as:
Count of participants · Participants
Number of Patients With Adverse Events and Serious Adverse Events
ParticipantsPhase 1b - Arm 1Phase 1b - Arm 2Phase 2 - Ombipepimut-S + Pembrolizumab
Number of Patients With Adverse Events and Serious Adverse Events7931
PrimaryDetermination of the Recommended Phase 2 Dose (RP2D) by Assessing Dose-limiting Toxicities (DLTs).

The RP2D was based on the data collected during phase 1b.

Time frame:
28 days
Reported as:
Number · mg
Determination of the Recommended Phase 2 Dose (RP2D) by Assessing Dose-limiting Toxicities (DLTs).
mgPhase 1b - Arm 2
Determination of the Recommended Phase 2 Dose (RP2D) by Assessing Dose-limiting Toxicities (DLTs).10.5
PrimaryPhase II: The Objective Response Rate (ORR) of DSP-7888 Dosing Emulsion Administered With Pembrolizumab in Patients With Platinum-resistant Ovarian Cancer (PROC).

Defined as the proportion of patients who have achieved confirmed Complete Response or Partial Response by RECIST v1.1 based on investigator assessment.

Time frame:
Radiographic imaging every 6 weeks for 24 weeks and then every 12 weeks until progression for an average of 12 months

No measurements were reported for this outcome.

SecondaryPhase Ib: The Objective Response Rate (ORR) of DSP-7888 Dosing Emulsion Administered With Pembrolizumab or Nivolumab

Defined as the proportion of patients who have achieved confirmed complete response (CR) or partial response (PR) evaluated using RECIST v1.1 and iRECIST.

Time frame:
At 4 weeks for the nivolumab arm and at 6 weeks for the pembrolizumab arm and then at Weeks 12, 18, and 24 after the first dose of the DSP-7888 dosing emulsion

No measurements were reported for this outcome.

SecondaryPhase Ib: The Disease Control Rate (DCR) of DSP-7888 Dosing Emulsion Administered With Pembrolizumab or Nivolumab

Defined as the percentage of patients who have achieved best overall response (BOR) of complete response (CR), partial response (PR), or stable disease (SD) per RECIST v1.1 and iRECIST.

Time frame:
At 4 weeks for the nivolumab arm and at 6 weeks for the pembrolizumab arm and then at Weeks 12, 18, and 24 after the first dose of the DSP-7888 dosing emulsion

No measurements were reported for this outcome.

SecondaryPhase Ib: Assessment of the Duration of Response (DOR) of Ombipepimut-S in Combination With Nivolumab or Pembrolizumab

DOR is defined as the time from first documentation of response until the time of first documentation of disease progression by RECIST v1.1 and iRECIST or death by any cause.

Time frame:
At week 4 for patients on the nivolumab arm and week 6 for patients on the pembrolizumab arm. Thereafter weeks 12, 18 and 24 and every 12 weeks until progression or death.

No measurements were reported for this outcome.

SecondaryPhase Ib: Progression-free Survival (PFS) of DSP-7888 Dosing Emulsion Administered With Pembrolizumab or Nivolumab

The percentage of participants with a complete response or partial response who have measurable disease at baseline imaging.

Time frame:
Radiographic imaging every 6 weeks for 24 weeks and then every 12 weeks until progression for an average of 12 months

No measurements were reported for this outcome.

SecondaryPhase Ib: The 6-month Progression-free Survival (PFS) Rate of Ombipepimut-S in Combination With Nivolumab or Pembrolizumab

Defined as the proportion of patients who neither progressed by RECIST (v.1.1) nor died before 6 months (24 weeks) from the first study treatment

Time frame:
6 months

No measurements were reported for this outcome.

SecondaryPhase Ib: Percentage of Patients With Overall Survival (OS) When Treated With Ombipepimut-S in Combination With Nivolumab or Pembrolizumab
Time frame:
12 months
Reported as:
Number · percentage of participants
Phase Ib: Percentage of Patients With Overall Survival (OS) When Treated With Ombipepimut-S in Combination With Nivolumab or Pembrolizumab
percentage of participantsPhase 1b - Arm 1Phase 1b - Arm 2
Phase Ib: Percentage of Patients With Overall Survival (OS) When Treated With Ombipepimut-S in Combination With Nivolumab or Pembrolizumab00
SecondaryPhase II: Assessment of the Duration of Response (DOR) of Ombipepimut-S in Combination With Pembrolizumab

Defined as the time from the first documentation of a response (CR or PR) until time of first documentation of disease progression by RECIST v1.1 or death by any cause.

Time frame:
Radiographic imaging every 6 weeks for 24 weeks and then every 12 weeks until progression up to 24 months.

No measurements were reported for this outcome.

SecondaryPhase II: Disease Control Rate of Ombipepimut-S in Combination With Pembrolizumab

Defined as the percentage of patients who have achieved best overall response (BOR) of complete response, partial response, or stable disease per RECIST (v.1.1)

Time frame:
Radiographic imaging every 6 weeks for 24 weeks and then every 12 weeks until progression, up to 24 months.

No measurements were reported for this outcome.

SecondaryPhase II: Assessment of the Progression-free Survival (PFS) of Ombipepimut-S in Combination With Pembrolizumab

Defined as the time from the date of the first dose of study treatment to the earlier date of assessment of progression by RECIST v.1.1, or death by any cause

Time frame:
Radiographic imaging every 6 weeks for 24 weeks and then every 12 weeks until progression, up to 24 months

No measurements were reported for this outcome.

SecondaryPhase II: 6-month Progression-free Survival (PFS) of Ombipepimut-S in Combination With Pembrolizumab

PFS is defined as the time from the date of the first dose of study treatment to the earlier date of assessment of progression by RECIST (v.1.1), or death by any cause

Time frame:
6 months

No measurements were reported for this outcome.

SecondaryPhase II: Overall Survival of Patients Treated With Ombipepimut-S in Combination With Pembrolizumab

Defined as the time from the date of first dose of study treatment to the date of death by any cause

Time frame:
Every 3 months from last dose of study treatment up to 24 months.

No measurements were reported for this outcome.

SecondaryPhase II: Immune Objective Response Rate (iORR) of Ombipepimut-S in Combination With Pembrolizumab

Defined as the percentage of patients who have achieved confirmed immune complete response (iCR) or immune partial response (iPR), evaluated using iRECIST based on investigator's assessment.

Time frame:
Up to 24 months

No measurements were reported for this outcome.

SecondaryPhase II: Immune Disease Control Rate (iDCR) of Ombipepimut-S in Combination With Pembrolizumab

Defined as the percentage of patients who have achieved best overall response of iCR, iPR, or immune stable disease (iSD), per iRECIST

Time frame:
Up to 24 months

No measurements were reported for this outcome.

SecondaryPhase II: Immune Progression-free Survival (iPFS) of Ombipepimut-S in Combination With Pembrolizumab

Defined as the time from the date of the first dose of study treatment to the earlier date of assessment of progression by iRECIST or death by any cause

Time frame:
Up to 24 months

No measurements were reported for this outcome.

SecondaryPhase II: Immune Duration of Response (iDOR) of Ombipepimut-S in Combination With Pembrolizumab

Defined as the time from the first documentation of response (iCR or iPR) until time of first documentation of disease progression by iRECIST, or death by any cause

Time frame:
Up to 24 months

No measurements were reported for this outcome.

SecondaryPhase II: Evaluation of the Safety and Tolerability of Ombipepimut-S in Combination With Pembrolizumab

Demonstrated by the number of participants with adverse events and serious adverse events

Time frame:
Up to 24 months

No measurements were reported for this outcome.

Adverse events

Collected over Serious and Other Adverse Events were assessed from the date of first treatment through 30 days of the last administration of study drug, an average of 12 months. All-Cause Mortality was assessed from the date of first treatment until death, an average of 24 months.. Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Phase 1b - Arm 11/7 (14.3%)3/7 (42.9%)7/7 (100%)
Phase 1b - Arm 20/9 (0%)5/9 (55.6%)9/9 (100%)
Phase 2 - Ombipepimut-S + Pembrolizumab1/31 (3.2%)8/31 (25.8%)31/31 (100%)
Most frequent serious events
Showing 10 of 27
Most frequent serious events
EventPhase 1b - Arm 1Phase 1b - Arm 2Phase 2 - Ombipepimut-S + Pembrolizumab
FallInjury, poisoning and procedural complications0/72/90/31
Small Intestinal ObstructionGastrointestinal disorders0/70/95/31
HypersensitivityImmune system disorders1/70/90/31
Spinal Cord CompressionNervous system disorders1/70/90/31
Acute Kidney InjuryRenal and urinary disorders1/70/91/31
PnemoniaInfections and infestations1/70/91/31
Pericardial EffusionCardiac disorders1/71/91/31
PyrexiaGeneral disorders0/71/90/31
SyncopeNervous system disorders0/71/90/31
Diabetic KetoacidosisMetabolism and nutrition disorders0/71/90/31
Most frequent other events
Showing 10 of 133
Most frequent other events
EventPhase 1b - Arm 1Phase 1b - Arm 2Phase 2 - Ombipepimut-S + Pembrolizumab
Injection Site ReactionGeneral disorders7/79/923/31
Injection Site PainGeneral disorders7/79/923/31
Decreased AppetiteGeneral disorders2/75/94/31
FatigueGeneral disorders2/74/915/31
NauseaGastrointestinal disorders1/72/913/31
ConstipationGastrointestinal disorders2/73/97/31
PyrexiaGastrointestinal disorders0/73/90/31
HypomagnesaemiaMetabolism and nutrition disorders0/73/96/31
Neck PainMusculoskeletal and connective tissue disorders0/73/90/31
Abdominal PainGeneral disorders0/70/910/31

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)Phase 1b - Arm 1Phase 1b - Arm 2Phase 2 - Ombipepimut-S + PembrolizumabTotal
<=18 years0000
Between 18 and 65 years451322
>=65 years341825
Sex: Female, Male
Sex: Female, Male(Participants)Phase 1b - Arm 1Phase 1b - Arm 2Phase 2 - Ombipepimut-S + PembrolizumabTotal
Female243137
Male55010
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Phase 1b - Arm 1Phase 1b - Arm 2Phase 2 - Ombipepimut-S + PembrolizumabTotal
American Indian or Alaska Native0011
Asian0022
Native Hawaiian or Other Pacific Islander0000
Black or African American0101
White782742
More than one race0011
Unknown or Not Reported0000
Region of Enrollment
Region of Enrollment(participants)Phase 1b - Arm 1Phase 1b - Arm 2Phase 2 - Ombipepimut-S + PembrolizumabTotal
United States793147
08

Study locations

19 sites
  • Arizona Oncology Associates, PC - HOPE
    Tucson, Arizona 85711, United States
  • Cedars-Sinai Medical Center
    Los Angeles, California 90048, United States
  • UC San Francisco Helen Diller Family Comprehensive Cancer Center
    San Francisco, California 94143, United States
  • Rocky Mountain Cancer Centers
    Aurora, Colorado 80012, United States
  • AdventHealth Cancer Institute
    Orlando, Florida 32804, United States
  • Decatur Memorial Hospital
    Decatur, Illinois 62526, United States
  • Horizon Oncology Research
    Lafayette, Indiana 47905, United States
  • Norton Cancer Institute
    Louisville, Kentucky 40241, United States
  • St Vincent Frontier Cancer Center
    Billings, Montana 59102, United States
  • Rutgers Cancer Institute of New Jersey
    New Brunswick, New Jersey 08901, United States
  • UC Health, LLC
    Cincinnati, Ohio 45229, United States
  • Ohio State University
    Columbus, Ohio 43210, United States
  • West Cancer Clinic
    Germantown, Tennessee 38138, United States
  • Mary Crowley Cancer Research
    Dallas, Texas 75251, United States
  • The University of Texas MD Anderson Cancer Center
    Houston, Texas 77030, United States
  • Seattle Cancer Care Alliance
    Seattle, Washington 98109, United States
  • Summit Cancer Centers
    Spokane, Washington 99208, United States
  • Centre hospitalier de l'Université de Montréal (CHUM)
    Montréal, Quebec H2X 0A9, Canada
  • SMBD Jewish General Hospital
    Montréal, Quebec H3T 1E2, Canada
09

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

10

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Dec 2017 to primary completion in Oct 2022, 58 months.

Results were first posted in Apr 2024, 1 year 5 months after primary completion.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 9, 2017
First posted
Oct 17, 2017
StartActual
Dec 14, 2017
Primary completionActual
Oct 19, 2022
CompletionActual
Nov 29, 2022
Results first posted
Apr 18, 2024
Last update
Apr 18, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 18, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT03311334
Responsible party
Sponsor
First posted
Oct 17, 2017
Start date
Dec 14, 2017
Primary completion
Oct 19, 2022
Completion
Nov 29, 2022
Results posted
Apr 18, 2024
Last update
Apr 18, 2024

Oversight

FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Mar 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Studies of the drug tested here: WT1 Protein-derived Peptide Vaccine DSP-7888

Start the discussion