ClinicalTrials.gg
RecruitingNCT07730021Updated Oct 26, 2026

A Study of ASP388B Given by Itself and With Standard Therapies in Participants With Solid Tumors

A Phase 1/2 interventional study of ASP388B and Pembrolizumab in Locally Advanced or Metastatic Solid Tumors, sponsored by Astellas Pharma Global Development, Inc.. Recruiting at 4 sites in 2 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-26.

Sponsored by Astellas Pharma Global Development, Inc. (part of Astellas Pharma Inc) · Phase 1/2, Interventional, and Treatment

From the registry’s dates

  • Started Sep 2026; still recruiting 2 months later.
Phase
Phase 1/2
Study type
Interventional
Enrollment
392
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 1,098 studies in Squamous Cell Carcinoma of Head and Neck with a site in United States — 216 open to participants now, 346 under way, 28 of them phase 3. Squamous Cell Carcinoma of Head and Neck · United States.

Planned enrollment
60th of 992
392 · median 41
Started
2026
with 58 others
Phase 1/2
157 of 1,098
42 open now
Primary completion
2030-02
later than 306 of 345 live
Registered
1,078th of 1,098
by date

Among the 1,098 studies in Squamous Cell Carcinoma of Head and Neck with a site in United States, this one is the 60th largest by planned enrollment of the 992 interventional ones that give a count, is one of 59 that started in 2026, is one of 157 in phase 1/2, reaches primary completion later than 306 of the 345 other live ones, and was the 1,078th registered.

Squamous Cell Carcinoma of Head and Neck

2,019 studies on the registry are indexed under Squamous Cell Carcinoma of Head and Neck; 573 are open to participants now.

Browse Squamous Cell Carcinoma of Head and Neck studies →

Open to participants now

216 of the 1,098 studies in Squamous Cell Carcinoma of Head and Neck with a site in United States are open now. Recruiting first, the newest first:

210 more — sign in →

All 216 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 433 Squamous Cell Carcinoma of Head and Neck studies recruiting now, 309 (71%) set no upper age limit and 87 (20%) stop at 75 or younger; 5 take children under 18; 13 take healthy volunteers.

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

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

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02

Study summary

This is an early development study of ASP388B in people with solid tumors. In this study, ASP388B will be given to people for the first time. It will be given by itself or together with standard cancer therapies. The main aims of the study are to check the safety of ASP388B and find the most suitable dose.

This study will be in 2 parts. In Part 1, different small groups of people with solid tumors will receive lower to higher doses of ASP388B. Some groups will receive ASP388B by itself, and other groups will receive ASP388B with standard cancer therapies. Any medical problems will be recorded for each dose. This is to find suitable doses of ASP388B to use in Part 2 of the study, and to include the tumor types that responded well to ASP388B.

In Part 2, other different small groups of people with the specific tumor types (from Part 1) will receive the most suitable doses worked out from Part 1. Some groups will receive ASP388B by itself, and other groups will receive ASP388B with standard cancer therapies.

In both parts of the study, ASP388B will be given once in 3-week cycles. The standard cancer therapies will be given according to their approved label. ASP388B and the standard cancer therapies will be given slowly through a tube into a vein. This is called an infusion.

In both parts of the study, health checks will be done at each visit, and the doctors will continue to check for medical problems throughout the study.

03

Conditions studied

  • Locally Advanced or Metastatic Solid Tumors

Keywords

  • ASP388B
  • Safety
  • Tolerability
  • Pembrolizumab
  • Carboplatin
  • 5-fluorouracil (5-FU)
  • Oxaliplatin
  • Head and Neck Squamous Cell Carcinoma (HNSCC)
  • Esophageal Squamous Cell Carcinoma (ESCC)
  • Metastatic castration-resistant prostate cancer(mCRPC)
  • Squamous non-small cell lung cancer (sqNSCLC)
  • Small cell lung cancer (SCLC)
04

Who can participate

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

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

For the ASP388B monotherapy dose escalation (excluding the tumor-specific backfill participants), the following criteria apply:

  • Participant has a confirmed diagnosis of locally advanced unresectable or solid tumors.
  • Participant has progressed on, is ineligible for, or has refused all available standard therapies (no limit to the number of prior treatment regimens).
  • Prior exposure to B7-H3, STING agonist or TopI directed therapy is allowed.
  • Participant must have one of the following (for all tumor types, any compounds of neuroendocrine histology is ineligible): HNSCC, ESCC, mCRPC, sqNSCLC, SCLC
  • For mCRPC

    • Participants with or cytologically confirmed mCRPC who are to a novel antiandrogen therapy (including but not limited to abiraterone, enzalutamide and/or apalutamide) and have failed at least 1 (but not more than 2) taxane regimens (or who are deemed medically unsuitable to be treated with a taxane regimen or have actively refused treatment with a taxane regimen).
    • Participants must have undergone bilateral orchiectomy or must be on continuous ADT with a GnRH agonist or antagonist.
    • Total serum testosterone ≤ 50 ng/dL or 1.7 nmol/L
    • Evidence of progressive disease, defined as ≥ 1 PCWG3 criteria: PSA level ≥ 1 ng/mL that has increased on at least 2 successive occasions at least 1 week apart; Nodal or visceral progression as defined by v1.1 with PCWG3 modifications; Appearance of ≥ 2 new lesions in bone scan
    • Participants with mCRPC can be enrolled without .
  • For sqNSCLC

    • Participants with known EGFR, ALK, ROS, BRAF or other actionable mutations are eligible if treated with mutation targeted therapy and have progressed, relapsed or discontinued treatment due to toxicity.
  • For SCLC

    • Metastatic or extensive stage (EC-SCLC)

For the ASP388B 2L+HNSCC monotherapy dose expansion (including the tumor-specific backfill participants from the monotherapy dose escalation), the following criteria apply:

  • Participant has histologically or cytologically confirmed HNSCC.

    • Tumors arising from the nasopharynx are excluded.
    • Known /PD-L1 status and any HPV status is eligible.
  • Participant has evidence of radiographic progression on or after the last regimen received.
  • Participant has locally advanced or metastatic disease that is not amenable to curative intent treatment.
  • Participant has progressed, relapsed or discontinued treatment due to toxicity after local guidelines/SOC regimen for locally advanced or metastatic disease, and has received ≤ 3 prior lines of anticancer therapy in the locally advanced or metastatic setting.

    • or adjuvant cytotoxic regimens will count as a prior regimen if relapsed or progressed ≤ 6 months after completion.
  • No prior exposure to B7-H3, STING agonist or TopI directed therapy is allowed.

For the ASP388B 2L+ESCC monotherapy dose expansion (including the tumor-specific backfill participants from the monotherapy dose escalation), the following criteria apply:

  • Participant has histologically or cytologically confirmed ESCC.

    • Known PD-1/PD-L1 status and any status is eligible.
  • Participant has evidence of radiographic progression on or after the last regimen received.
  • Participant has locally advanced or metastatic disease that is not amenable to curative intent treatment.
  • Participant has progressed, relapsed or discontinued treatment due to toxicity after local guidelines/SOC regimen for locally advanced or metastatic disease, and has received ≤ 3 prior lines of anticancer therapy in the locally advanced or metastatic setting.

    • Neoadjuvant or adjuvant cytotoxic regimens will count as a prior regimen if relapsed or progressed ≤ 6 months after completion.
  • No prior exposure to B7-H3, STING agonist or TopI directed therapy is allowed.

For the ASP388B 1L HNSCC (Excluding NPC and Salivary Gland Tumors) combination therapy dose escalation and expansion (including the tumor-specific backfill participants from combination therapy dose escalation), the following criteria apply: (ASP388B + Pembrolizumab + Carboplatin + 5-FU):

  • Participant has histologically or cytologically confirmed HNSCC excluding nasopharyngeal cancer (NPC) and salivary gland tumors.

    • Known PD-1/PD-L1 status and any HPV status is eligible
  • Participant has recurrent or metastatic disease that is incurable by local therapies.
  • Participant has had no prior systemic therapy administered with the exception of systemic therapy completed > 6 months prior if given as part of multimodal treatment with curative intent for nonmetastatic disease stages.
  • No prior exposure to B7-H3, STING agonist or TopI directed therapy is allowed.

For the ASP388B 1L ESCC combination therapy dose escalation and expansion (including the tumor-specific backfill participants from combination therapy dose escalation), the following criteria apply: (ASP388B + Pembrolizumab + Oxaliplatin + 5-FU):

  • Participant has histologically or cytologically confirmed ESCC.

    • Known PD-1/PD-L1 status and any HER2 status is eligible
  • Participant has had no prior systemic therapy administered with the exception of systemic therapy completed > 6 months prior if given as part of multimodal treatment with curative intent for nonmetastatic disease stages.
  • No prior exposure to B7-H3, STING agonist or TopI directed therapy is allowed.

For the ASP388B 1L ESCC combination therapy dose escalation and expansion

  • Participant has a predicted ≥ 12 weeks.
  • Participant has at least 1 measurable lesion per RECIST v1.1. Lesions situated in a previously irradiated area are considered measurable if progression has been demonstrated in such lesions.
  • Participant has an performance status of 0 or 1.
  • Participant has adequate organ function as indicated by laboratory values (If a participant has received a recent blood transfusion, the laboratory tests must be obtained ≥ 14 days after any blood transfusion).
  • Female participant is not pregnant and at least 1 of the following conditions apply:

    • Not a woman of (WOCBP)
    • WOCBP who has a negative urine or serum pregnancy test at screening with a medical interview and agrees to follow the guidance from the time of through at least 7 months after final study intervention administration or after at least 9 months for participants with 1L ESCC receiving combination therapy, or per local labeling requirements, whichever is longer.
  • Female participant must not be breastfeeding or lactating starting at screening and throughout the period and for 5 half-lives (approximately 7 months after final study intervention administration or after at least 9 months for participants with 1L ESCC receiving combination therapy, or per local labeling requirements, whichever is longer).
  • Male participant must agree to use contraception with female partner(s) of childbearing potential (including breastfeeding partner) throughout the treatment period and for 4 months after final study intervention administration or after at least 9 months for participants with 1L ESCC receiving combination therapy, or per local labeling requirements, whichever is longer.
  • Male participant must agree to remain abstinent or use a condom with pregnant partner(s) for the duration of the pregnancy throughout the investigational period and for 4 months after final study intervention administration or after at least 9 months for participants with 1L ESCC receiving combination therapy, or per local labeling requirements, whichever is longer.

Exclusion criteria

Exclusion Criteria:

  • Participant weighs \< 40 kg during screening.
  • Participant has known active central nervous system (CNS) . NOTE: A participant with who has been treated with surgery and/or radiation therapy, who is no longer taking pharmacologic doses of and is neurologically stable, is eligible. Prophylactic use of anticonvulsants is permitted.
  • Participant has any of the following:

    • Any history of recurrent Grade 3 immune-related AEs (irAEs) or history of Grade 4 irAEs related to prior anticancer therapy.
  • Participant has active or prior or inflammatory disorders requiring systemic therapy within the past 2 years including inflammatory skin conditions, inflammatory bowel disease (e.g., ulcerative colitis or Crohn's disease), diverticulitis (with the exception of diverticulosis), celiac disease, systemic lupus erythematosus, Sarcoidosis syndrome, Wegener syndrome (granulomatosis with polyangiitis), Graves' disease, rheumatoid arthritis, hypophysitis or uveitis. The following are exceptions to this criterion:

    • Participant with type 1 diabetes mellitus
    • Participant with vitiligo or alopecia
    • Participant with endocrinopathies stably maintained on appropriate replacement therapy
    • Participant with any chronic skin condition that does not require systemic therapy
  • Participant has as a manifestation of the current .
  • Participant has a known additional malignancy that requires active treatment, with the exception of any of the following:

    • Adequately treated basal or squamous cell skin cancer, superficial bladder cancer or carcinoma in situ of the cervix or breast
    • Adequately treated stage I cancer from which the participant is currently in remission and has been in remission for ≥ 2 years
    • Any other cancer from which the participant has been disease-free for ≥ 5 years
  • Participant has a known history of infection with AIDS-related complications. HIV testing will be conducted per local requirements.
  • Participant has cardiac disease, defined as any of the following:

    • Clinically significant cardiac arrhythmias, including bradyarrhythmia and ventricular arrhythmia, which are poorly controlled; cardiomyopathy or moderate or severe valvular disease. NOTE: Rate-controlled atrial fibrillation is permitted.
    • Congenital long syndrome.
    • QTcF ≥ 470 msec at screening. ECGs will be performed in triplicate during screening; the average of the triplicate readings will be used in the calculation of QTcF. If the QTcF is prolonged in a participant with a pacemaker or a right-sided bundle branch block, the participant may be enrolled in the study if confirmed by the sponsor's medical monitor. Participant with a left-sided bundle branch block will be excluded.
    • History of clinically significant cardiac disease or congestive heart failure greater than Class II or measurement of \< 50% at baseline. Participant must not have had acute coronary syndrome, new-onset angina or coronary revascularization (PCI/CABG) within the past 12 months.
    • Uncontrolled hypertension, defined as systolic BP > 160 mmHg or diastolic BP > 100 mmHg that has been confirmed by 2 successive measurements, despite optimal medical management.
    • Arterial or venous thrombotic or embolic events such as cerebrovascular accident (including ), deep vein thrombosis or pulmonary embolism within the 3 months before start of study intervention.
    • Presence of cardiac injury syndromes: recent cardiac surgery, pacemaker/implantable cardioverter defibrillator insertion, ablation within 3 months prior to screening, recent PCI, blunt or penetrating chest trauma
    • Presence or history of pericarditis (acute, recurrent or restrictive), myocarditis or any pericardial effusion requiring drainage or other invasive procedures
    • History of pericardial tamponade, pericardial involvement associated with connective tissue diseases, sarcoidosis, vasculitis; congenital absence of defect of pericardium; aortic dissection with blood tracking into the pericardial space (hemopericardium/tamponade); iatrogenic hemopericardium (e.g., catheter perforation)
    • Significantly elevated cardiac biomarkers (troponins and NT-proBNP) that require cardiology referral at screening
  • Participant has a history of pleurodesis with impaired lung mechanics, recent (\< 6 weeks) pleurodesis or pleural surgery (decortication, pleurectomy), drug-induced fibrosing ILD, trapped lung, complicated pleural effusion, uncontrolled malignant pleural effusion, idiopathic pulmonary fibrosis, pneumonectomy, organizing pneumonia, drug-induced pneumonitis, idiopathic pneumonitis, noninfectious ILD/pneumonitis, fibrotic lung disease or connective tissue disorder with pulmonary involvement. Any participant with a history of radiation pneumonitis that required treatment (e.g., steroid) will be excluded, regardless of resolution. NOTE: Participant with previously diagnosed Grade 1 radiation pneumonitis is allowed to be screened for the study. However, radiation pneumonitis must be confined to the previously irradiated area of the lung and be completely resolved.
  • Participant has current Grade ≥ 1 ILD/pneumonitis, evidence of active pneumonitis on screening chest CT scan, or suspected ILD/pneumonitis that cannot be ruled out by imaging at screening. NOTE: If participant requires intermittent use of bronchodilators, inhaled steroids or local steroid injections, they will not be excluded.
  • Participant has pericardial disease related to prior radiation therapy.
  • Participant has a confirmed SpO2 \< 92% at screening.
  • Participant requires chronic oxygen supplementation therapy inclusive of noninvasive ventilation or bilevel positive airway pressure.
  • Participant has any lung or heart disease (e.g., asthma, , congestive heart failure) with uncontrolled symptoms or recent exacerbation or which may confound pulmonary safety assessments.
  • Participant is at a significant risk of bleeding due to medical condition(s) or recent major bleeding (e.g., bleeding in critical site or requiring transfusions).
  • Participant has current peripheral neuropathy Grade ≥ 2 (specific for platinum-containing cohorts only).
  • Participant has a history of Grade ≥ 2 hearing loss (specific for platinum-containing cohorts only).
  • Participant has received any strong inhibitors of and CYP1A2 within 1 week or 5 half-lives (whichever is longer) or strong inducers of CYP3A within 2 weeks or 5 half-lives (whichever is longer) before the first dose of ASP388B.
  • Participant has received prior B7-H3 targeting agents, STING agonists or TopI inhibitor (exception: monotherapy dose escalation cohorts).
  • Participant has received prior radiation therapy within 2 weeks of the first dose of study intervention. Participant must have recovered from all radiation-related toxicities and not require corticosteroids. A 1-week is permitted for palliative radiation (≤ 3 weeks of radiotherapy) to non-CNS disease.
  • Participant is receiving anticoagulants (vitamin K antagonists or direct oral anticoagulants) or antiplatelet agents. Low dose aspirin is allowed.
  • Participant has received prior immuno-oncology anticancer therapy within 6 weeks prior to the first dose of study intervention. Participant has received any other prior anticancer therapy within 28 days or 5 half-lives, whichever is longer, of the first dose of study intervention.
Terms in these criteria, in plain language(28)

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.

Metastases

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

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.

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.

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.

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.

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.

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.

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.

HER2

HER2 is a protein, made from the ERBB2 gene, that drives the growth of some cancers. A study may look for a level of the protein, extra copies of the gene, or a particular change in it.

In breast cancer, protein tests are read as HER2-positive, HER2-low or HER2-negative; other cancers use their own rules. Check which test result the study requires.

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.

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.

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.

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.

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.

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.

Leptomeningeal disease

Cancer that has spread to the leptomeninges, the thin layers covering the brain and spinal cord, and the fluid between them. It is not the same as brain metastases.

Criteria often treat it separately, and many studies leave it out even where treated brain metastases are allowed.

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.

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.

NYHA class (heart failure)

The New York Heart Association’s four classes of how much heart failure limits physical activity.

I
No limits: ordinary activity causes no undue tiredness or breathlessness.
II
Slight limits: comfortable at rest, ordinary activity causes symptoms.
III
Marked limits: comfortable at rest, less than ordinary activity causes symptoms.
IV
Symptoms even at rest; any activity makes them worse.

Studies set their own limit — many outside heart failure leave out class III–IV, while heart failure studies may ask for a particular class. Check the class this study names.

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.

TIA (transient ischaemic attack)

A “mini-stroke”: temporary stroke-like symptoms caused by reduced blood flow to part of the brain, spinal cord or eye, without signs of a new stroke on a scan.

Stroke symptoms need emergency care at once, even if they go away.

COPD

Chronic obstructive pulmonary disease: long-term lung disease that makes it hard to breathe out, including emphysema and chronic bronchitis.

CYP3A (CYP3A4) inhibitors and inducers

CYP3A is a group of enzymes, mainly CYP3A4, in the liver and gut that break down many medicines. Some medicines, supplements and foods (grapefruit, St John’s wort) slow them down or speed them up, which changes how much of a study drug stays in the body.

Studies list them so they can be avoided or switched; bring a list of everything you take, including supplements.

Washout period

A planned gap after a treatment, so that its effects can lessen before the study treatment or a study assessment. Ask the study team and the doctor who prescribed it before changing any medicine.

05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
392 participants (estimated)

Study arms

  • Experimental
    ASP388B Monotherapy Dose Escalation

    Participants with head and neck squamous cell carcinoma (HNSCC) \[including nasopharyngeal cancer (NPC)\], esophageal squamous cell carcinoma (ESCC), metastatic castration-resistant prostate cancer(mCRPC), squamous non-small cell lung cancer (sqNSCLC) or small cell lung cancer (SCLC) will receive the dose based on the assigned dose level of ASP388B in 21-day cycles.

    Drug: ASP388B

  • Experimental
    ASP388B Monotherapy Dose Expansion (HNSCC)

    Participants with HNSCC excluding NPC, will receive ASP388B in 21-day cycles with dose level(s) selected from dose escalation.

    Drug: ASP388B

  • Experimental
    ASP388B Monotherapy Dose Expansion (ESCC)

    Participants with ESCC will receive ASP388B in 21-day cycles with dose level(s) selected from dose escalation.

    Drug: ASP388B

  • Experimental
    ASP388B Combination Therapy Dose Escalation (HNSCC)

    Participants with HNSCC excluding NPC and salivary gland tumors will receive ASP388B in 21-day cycles at dose level(s) based on emerging data.

    Drug: ASP388B · Drug: Pembrolizumab · Drug: Carboplatin · Drug: 5-fluorouracil

  • Experimental
    ASP388B Combination Therapy Dose Escalation (ESCC)

    Participants with ESCC will receive ASP388B in 21-day cycles at dose level(s) based on emerging data.

    Drug: ASP388B · Drug: Pembrolizumab · Drug: Oxaliplatin · Drug: 5-fluorouracil

  • Experimental
    ASP388B Combination Therapy Dose Expansion (HNSCC)

    Participants with HNSCC excluding NPC and salivary gland tumors will receive ASP388B in 21-day cycles at dose level(s) based on emerging data.

    Drug: ASP388B · Drug: Pembrolizumab · Drug: Carboplatin · Drug: 5-fluorouracil

  • Experimental
    ASP388B Combination Therapy Dose Expansion (ESCC)

    Participants with ESCC will receive ASP388B in 21-day cycles at dose level(s) based on emerging data.

    Drug: ASP388B · Drug: Pembrolizumab · Drug: Oxaliplatin · Drug: 5-fluorouracil

Interventions

06

What researchers measure

Primary outcomes

  1. Number of Participants with Dose Limiting Toxicities (DLTs)

    A DLT is defined as any event meeting the DLT criteria occurring within 21 days of first dose on Cycle 1 Day 1 (C1D1) that cannot clearly be attributed to a cause other than ASP388B administered in monotherapy or in combination with standard treatments.

    Time frame: Up to 21 days after C1D1

  2. Number of Participants with Treatment-Emergent Adverse Events (TEAEs)

    An AE is any untoward medical occurrence in a patient or clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention. NOTE: An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom or disease (new or exacerbated) temporally associated with the use of study intervention. This includes events related to the comparator, if applicable, and events related to the (study) procedures. A TEAE is an AE with onset at any time from first dosing until last scheduled procedure.

    Time frame: Up to 45 months

  3. Number of participants with laboratory value abnormalities and/or adverse events (AEs)

    Number of participants with potentially clinically significant laboratory values.

    Time frame: Up to 45 months

  4. Number of participants with vital sign abnormalities and/or AEs

    Number of participants with potentially clinically significant vital sign values.

    Time frame: Up to 45 months

  5. Number of participants with electrocardiogram (ECG) abnormalities and/or AEs

    Number of participants with potentially clinically significant ECG values.

    Time frame: Up to 45 months

  6. Number of Participants with Physical Examination (PE) abnormalities and/or AEs

    Number of participants with potentially clinically significant PE values.

    Time frame: Up to 45 months

  7. Number of Participants at each grade of Eastern Cooperative Oncology Group (ECOG) performance status score

    The ECOG scale will be used to assess performance status. Scores range from 0 (fully active) to 5 (dead). Negative change scores represent an improvement. Positive scores represent a decline in performance.

    Time frame: Up to 45 months

Secondary outcomes

  1. Objective Response Rate (ORR) of ASP388B per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1

    ORR is defined as the proportion of participants whose best overall response with confirmation is rated as Complete Response (CR) or Partial Response (PR) per RECIST v1.1 as assessed by investigator. All tumor types except mCRPC.

    Time frame: Up to 45 months

  2. Objective Response Rate (ORR) of ASP388B per Prostate Cancer Working Group 3 (PCWG3)

    ORR is defined as the proportion of participants whose best overall response with confirmation is rated as Complete Response (CR) or Partial Response (PR) per PCWG3 guidance as assessed by the investigator. mCRPC only.

    Time frame: Up to 45 months

  3. Duration of Response (DOR) of ASP388B per RECIST v1.1

    DOR is for responders only. DOR is defined as the time from when the measurement criteria is first met for BOR rated as CR or PR (whichever is first recorded) until the first date of documented radiological disease progression by investigator per RECIST v1.1 or death in the absence of progression. All tumor types except mCRPC.

    Time frame: Up to 45 months

  4. Duration of Response (DOR) of ASP388B per Prostate Cancer Working Group (PCWG3)

    DOR is for responders only. DOR is defined as the time from when the measurement criteria are first met for BOR rated as CR or PR (whichever is first recorded) until the first date of documented radiological disease progression by investigator per PCWG3 guidance or death in the absence of progression. mCRPC only.

    Time frame: Up to 45 months

  5. Disease Control Rate (DCR) of ASP388B per RECIST v1.1

    DCR is defined as the proportion of participants whose best overall response (BOR) with confirmation is rated as CR, PR or stable disease (SD) per RECIST v1.1 as assessed by the investigator. All tumor types except mCRPC.

    Time frame: Up to 45 months

  6. Disease Control Rate of ASP388B per Prostrate Cancer Working Group 3 (PCWG3)

    DCR is defined as the proportion of participants whose BOR with confirmation is rated as CR, PR or stable disease (SD) per PCWG3 guidance as assessed by the investigator. mCRPC only.

    Time frame: Up to 45 months

  7. Pharmacokinetics (PK) of ASP388B Total Antibody (TAb) in plasma: area under the concentration-time curve at 21 days (AUC21d)

    AUC21d will be recorded from the PK plasma samples collected.

    Time frame: Up to 12 months

  8. PK of ASP388B TAb in plasma: maximum concentration (Cmax)

    Cmax will be recorded from the PK plasma samples collected.

    Time frame: Up to 12 months

  9. PK of ASP388B TAb in plasma: trough concentration (Ctrough)

    Ctrough will be recorded from the PK plasma samples collected.

    Time frame: Up to 12 months

  10. PK of ASP388B TAb in plasma: time of maximum concentration (tmax)

    tmax will be recorded from the PK plasma samples collected.

    Time frame: Up to 12 months

  11. Change from baseline in CD8 T-cell lymphocytes

    CD8 T-cell lymphocytes will be measured from the tumor tissue samples collected.

    Time frame: Baseline up to 18 months

  12. Number of Participants with Anti-drug Antibodies (ADA) against ASP388B

    ADA will be recorded from the serum samples collected.

    Time frame: Up to 16 months

07

Study locations

4 of 4 sites recruiting
08

References and documents

Individual participant data

Plan to share: Yes — Access to anonymized individual participant level data collected during the study, in addition to study-related supporting documentation, is planned for studies conducted with approved product indications and formulations, as well as products terminated during development. Studies conducted with product indications or formulations that remain active in development are assessed after study completion to determine if Individual Participant Data can be shared. Further details on Astellas' data sharing policy can be found at https://www.clinicaltrials.astellas.com/transparency/.

Supporting information: Study protocol, Statistical analysis plan, Clinical study report

Time frame: Access to participant level data is offered to researchers after publication of the primary manuscript (if applicable) and is available as long as Astellas has legal authority to provide the data.

Access criteria: Researchers must submit a proposal to conduct a scientifically relevant analysis of the study data. The research proposal is reviewed by an Independent Research Panel. If the proposal is approved, access to the study data is provided in a secure data sharing environment after receipt of a signed Data Sharing Agreement.

Data sharing details ↗ · www.clinicaltrials.astellas.com

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Sep 2026 (actual). Primary completion is estimated for Feb 2030, 41 months after the start.

Of 93 industry-sponsored phase 1/2 interventional studies under Squamous Cell Carcinoma of Head and Neck, half reached primary completion within 60 months of starting (the median), counting those still running; a quarter within 44 and three quarters within 78. This study's planned 41 months is below that.

Counting every sponsor, half of 138 studies reached it within 61 months; a quarter within 47 and three quarters within 82.

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

Registered
Jul 23, 2026
First posted
Jul 28, 2026
StartActual
Sep 2, 2026
Primary completionEst.
Feb 28, 2030
CompletionEst.
May 31, 2030
Last update
Oct 26, 2026
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.
Minor edits
Nothing that changes what the study is or who can join. Edited: verification date and description
1 update, last Oct 26, 2026
Show all 1 update
  1. Oct 26, 2026
    Minor edits only
    + 2 other changes: verification date and description

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07730021
Responsible party
Sponsor
First posted
Jul 28, 2026
Start date
Sep 2, 2026
Primary completion
Feb 28, 2030 (estimated)
Completion
May 31, 2030 (estimated)
Last update
Oct 26, 2026

Study contacts

Astellas Pharma Global Development, Inc.
Contact
Astellas.registration@astellas.com
800-888-7704
Medical Monitor
study director · Astellas Pharma Global Development, Inc.

Oversight

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

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