ClinicalTrials.gg
RecruitingNCT04752826Updated Sep 18, 2026

BI-1808 as a Single Agent and With Pembrolizumab (KEYTRUDA® ) in Treatment of Advanced Malignancies(Keynote-D20)

A Phase 1/2 interventional study of BI-1808 and Pembrolizumab (KEYTRUDA® ) 25 Mg/mL Solution for Injection in Advanced Malignancies, Ovarian Cancer and T-cell Lymphoma, sponsored by BioInvent International AB. Recruiting at 25 sites in 7 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-18.

Sponsored by BioInvent International AB · Phase 1/2, Interventional, and Treatment

From the registry’s dates

  • Started Jan 2021; still recruiting 5 years 9 months later.
Phase
Phase 1/2
Study type
Interventional
Enrollment
250
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 292 studies in Ovarian Neoplasms with a site in United Kingdom — 54 open to participants now, 85 under way, 24 of them phase 3. Ovarian Neoplasms · United Kingdom.

Planned enrollment
91st of 248
250 · median 159
Started
2021
with 21 others
Phase 1/2
41 of 292
13 open now
Primary completion
2028-01
later than 54 of 84 live
Registered
216th of 292
by date

Among the 292 studies in Ovarian Neoplasms with a site in United Kingdom, this one is the 91st largest by planned enrollment of the 248 interventional ones that give a count, is one of 22 that started in 2021, is one of 41 in phase 1/2, reaches primary completion later than 54 of the 84 other live ones, and was the 216th registered.

Ovarian Neoplasms

3,381 studies on the registry are indexed under Ovarian Neoplasms; 790 are open to participants now.

Browse Ovarian Neoplasms studies →

Open to participants now

54 of the 292 studies in Ovarian Neoplasms with a site in United Kingdom are open now. Recruiting first, the newest first:

49 more — sign in →

All 54 open studies →

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

Who these studies take

Of the 606 Ovarian Neoplasms studies recruiting now, 443 (73%) set no upper age limit and 107 (18%) stop at 75 or younger; 39 take children under 18; 45 take healthy volunteers.

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

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02

Study summary

The goal of this first in human clinical trial is to test BI-1808 administered as single agent and in combination with pembrolizumab in subjects with advanced malignancies whose disease has progressed after standard therapy.

The main questions it aims to answer are:

  • how safe and tolerable is BI-1808
  • what is maximum tolerated or administrated dose
  • to determine recommended dose for further clinical trials. Participants will receive infusions of with BI-1808 as a single agent, BI-1808 in combination with pembrolizumab and BI-1808 in combination with pembrolizumab and paclitaxel every 3 weeks.

For the purpose of this study, subjects with advanced malignancies includes subjects with advanced solid tumors and subjects with T-cell lymphoma (TCL),

Read the detailed description

This is a Phase 1/2a, dose-escalation, multicenter, first-in-human, consecutive-cohort, open-label study of BI-1808, as a single agent, in combination with pembrolizumab, and in BI-1808 in combination with pembrolizumab and paclitaxel in subjects with advanced malignancies, whose disease has progressed after standard therapy.

The study will consist of 2 phases: a Phase 1 with Parts A and B, and a Phase 2a with Parts A , B and C.

Phase 1 Part A consists of a dose escalation of BI-1808 as a single agent to evaluate safety and tolerability and to determine the RP2D as a single agent (sRP2D) in subjects with advanced malignancies whose disease has progressed after standard therapy.

Phase 1 Part B consists of a dose escalation of BI-1808 in combination with pembrolizumab to evaluate the safety and tolerability of the combination treatment and to allow selection of the RP2D for BI-1808 in combination with pembrolizumab (cRP2D) in subjects with advanced malignancies whose disease has progressed after standard therapy.

Phase 2a will assess BI-1808 administered as a single agent (Part A), in combination with pembrolizumab (Part B), and in combination with pembrolizumab and paclitaxel (Part C) at the respective hypothesized RP2D(s) determined in Phase 1. Phase 2a expansion will be conducted in indication specific signal seeking cohorts and indication specific Dose Optimization Cohorts) of subjects. The Phase 2a study aims to further evaluate the safety and tolerability of BI-1808 as monotherapy (Part A), in combination with pembrolizumab (Part B), and in combination with pembrolizumab and paclitaxel (Part C). Including characterization of the PK and PD profiles of BI-1808, evaluation of preliminary antitumor activity based on ORR, DoR, and progression-free survival (PFS) as assessed by RECIST v1.1 and iRECIST, and determination of the recommended Phase 2 dose (RP2D).

03

Conditions studied

  • Advanced Malignancies
  • Ovarian Cancer
  • T-cell Lymphoma
  • Melanoma

Keywords

  • Advanced Malignancies
  • T-cell Lymphoma
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

  • Able and willing to provide written .
  • Aged 18 years or older.
  • confirmed advanced or eligible for an enrolling study cohort.
  • Disease progression following, intolerance of, ineligibility for, or refusal of applicable standard therapy.
  • At least one according to the response criteria specified in the protocol.
  • performance status of 0 or 1.
  • of at least 12 weeks.
  • Adequate organ function.
  • Willing and medically suitable to provide required tumor or skin .
  • Meets the disease-specific and treatment-history requirements of the applicable Phase 2a cohort.
  • For Phase 2a Part C: Histologically confirmed platinum-resistant high-grade serous or clear-cell ovarian carcinoma, prior platinum-based treatment as specified in the protocol, and suitability for paclitaxel treatment.

Exclusion criteria

Exclusion Criteria:

1. Active central nervous system or carcinomatous meningitis.

  • Active or disease, immunodeficiency, or use of prohibited treatment.
  • Prior treatment-related toxicity not recovered to the level specified in the protocol.
  • Prior anticancer therapy, radiotherapy, immunotherapy, treatment, or within the protocol-defined .
  • History of clinically significant immune-mediated toxicity, including pneumonitis, associated with previous immune- treatment.
  • Uncontrolled or clinically significant cardiovascular disease, serious infection, or another condition that could compromise safety or study participation.
  • Major surgery without adequate recovery.
  • Prior allogeneic tissue or solid-organ transplantation or active .
  • Pregnancy or breastfeeding, or unwillingness to comply with protocol-defined requirements.
  • Known to a study treatment or its components.
  • Another active , except for protocol-defined permitted malignancies.
  • Participation in another interventional clinical trial that conflicts with this study.
  • Unable or unlikely to comply with study procedures and requirements.
  • For Phase 2a Part C: Receipt of prohibited colony-stimulating factors within the protocol-defined period before treatment.
Terms in these criteria, in plain language(18)

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

GVHD (graft-versus-host disease)

After a transplant from a donor, the donor’s immune cells attack the recipient’s body, often the skin, gut or liver.

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.

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.

05

Study design

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

Study arms

  • Experimental
    Phase I, Part A - Dose escalation and safety of BI-1808 as single agent

    Dose escalation of BI-1808 administrated a single agent

    Drug: BI-1808

  • Experimental
    Phase I, Part B - Dose escalation and Safety of BI-1808 in combination with pembrolizumab

    Dose escalation of BI-1808 in combination with pembrolizumab.

    Drug: BI-1808 · Drug: Pembrolizumab (KEYTRUDA® ) 25 Mg/mL Solution for Injection

  • Experimental
    Phase 2a - Part A dose expansion of BI-1808 as a single agent

    BI-1808 administered as a single agent at the hypothesized recommended phase 2 dose determined in Phase 1

    Drug: BI-1808

  • Experimental
    Phase 2a, Part B - Dose expansion of BI-1808 in combination with pembrolizumab

    BI-1808 administered in combination with pembrolizumab at the respective hypothesized recommended phase 2 doses determined in Phase 1

    Drug: BI-1808 · Drug: Pembrolizumab (KEYTRUDA® ) 25 Mg/mL Solution for Injection

  • Experimental
    Phase 2a, Part C - Dose expansion of BI-1808 in combination with pembrolizumab and paclitaxel

    BI-1808 administered in combination with pembrolizumab and paclitaxel at the respective hypothesized recommended phase 2 doses determined in Phase 1.

    Drug: BI-1808 · Drug: Pembrolizumab (KEYTRUDA® ) 25 Mg/mL Solution for Injection · Drug: Paclitaxel 80 mg/m2 weekly

Interventions

  • DrugBI-1808

    BI-1808 administered as a flat-dose IV infusion once every 3 weeks

  • DrugPembrolizumab (KEYTRUDA® ) 25 Mg/mL Solution for Injection

    Drug page: Pembrolizumab

    Pembrolizumab administered as a flat-dose IV infusion once every 3 weeks.

  • DrugPaclitaxel 80 mg/m2 weekly

    Drug page: Paclitaxel

    Paclitaxel administered as a flat-dose IV infusion weekly.

06

What researchers measure

Primary outcomes

  1. Occurrence of adverse events (AEs)

    AEs will be assessed by the investigators by severity and will be graded according to the NCI CTCAE v5.0 or higher and causality between AEs and the exposure to the study treatment.

    Time frame: From the start of the study treatment for up to 2 years and 90 days.

  2. Identify DLTs, determine the maximum tolerated dose and select a recommended Phase 2 dose (RP2D) of BI-1808, given via intravenous (IV) infusion, as a single agent (Phase 1, Part A), and in combination with pembrolizumab (Phase 1, Part B)

    Determine the hypothesized RP2D dose for BI-1808 Phase 2a according to mTPI-2 design

    Time frame: Up to 104 weeks (2 years)

  3. Occurrence of serious adverse events (SAEs)

    SAEs will be assessed by the investigators by severity and will be graded according to the NCI CTCAE v5.0 or higher and causality between SAEs and the exposure to the study treatment

    Time frame: Up to 104 weeks (2 years)

  4. To identify the recommended Phase 2 dose (RP2D) of BI-1808,

    Select the RP2D dose for BI-1808 derived from the totality of PK, PD, clinical response, safety,and tolerability observed in signal seeking and dose optimization cohorts.

    Time frame: up to 104 weeks (2 years)

Secondary outcomes

  1. Evaluation of PK parameters for BI-1808. Maximum observed plasma concentration (Cmax)

    Study the PK profile of BI-1808 according to a non-compartmental analysis using a validated software

    Time frame: Up to 104 weeks (2 years)

  2. Evaluation of ADA response to BI-1808 in serum with validated method

    The detection and characterization of antibodies to BI-1808 will be performed using a validated method and will be evaluated for BI-1808 serum concentration to enable interpretation of the antibody data

    Time frame: Up to 104 weeks (2 years)

  3. Measurement of TNFR2 receptor occupancy on CD14+ and/CD16+ cells in serum with validated method

    evaluate the receptor occupancy of BI-1808 as a single agent and in combination with pembrolizumab or pembrolizumab and paclitaxel on T-cells expressing TNFR2 in absolute value

    Time frame: Up to 104 weeks (2 years)

07

Study locations

18 of 25 sites recruiting
  • City of Hope National Medical Center
    Duarte, California 91010, United States
    Recruiting
    • Christiane Querfeld · Principal investigator
  • Memorial Sloan Kettering Cancer Center
    New York, New York 10021, United States
    Recruiting
    • Jasmine Zain · Contact
  • University of Pennsylvania
    Philadelphia, Pennsylvania 19104, United States
    Recruiting
    • Stefan Barta · Principal investigator
  • Rigshospitalet
    Copenhagen, Denmark
    Recruiting
    • Kristoffer Staal Rohrberg · Principal investigator
  • Herlev Hospital
    Herlev, 2730, Denmark
    Recruiting
    • Rikke Løvendahl Eefsen · Principal investigator
  • PRA Health Sciences - Hungary
    Budapest, 1077, Hungary
    Active, not recruiting

    Not enrolling at this site — choose another above.

  • Magyar Honvédség-Egészségügyi Központ
    Budapest, 1134, Hungary
    Recruiting
    • Zsuzsanna Pápai · Principal investigator
  • Debreceni Egyetem Klinikai Központ
    Debrecen, 4032, Hungary
    Withdrawn

    Not enrolling at this site — choose another above.

  • Byudzhetnoye Uchrezhdeniye Zdravookhraneniya Omskoy Oblasti - Klinicheskiy Onkologicheskiy Dispanser
    Omsk, 644013, Russia
    Terminated

    Not enrolling at this site — choose another above.

  • National Medical Research Center VA Almazov
    Saint Petersburg, 197022, Russia
    Withdrawn

    Not enrolling at this site — choose another above.

  • N.N. Petrov National Medical Research Center of Oncology
    Saint Petersburg, 197758, Russia
    Withdrawn

    Not enrolling at this site — choose another above.

  • Institut Catala d'oncologia. Hospital Duran I Reynals
    Barcelona, 08907, Spain
    Not yet recruiting
  • Hospital Universitario Puerta de Hierro-Majadahonda, Madrid,
    Madrid, 28007, Spain
    Not yet recruiting
  • START Madrid - Hospital Universitario Fundación Jiménez Díaz
    Madrid, 28040, Spain
    Recruiting
  • Hospital Universitario 12 de Octubre
    Madrid, 28041, Spain
    Recruiting
  • Sahlgrenska University Hospital
    Gothenburg, 41345, Sweden
    Recruiting
    • Edvard Abel · Principal investigator
  • Skanes University Hospital
    Lund, 223 70, Sweden
    Recruiting
    • Ana Carnerio · Principal investigator
  • Karolinska University Hospital, Solna
    Stockholm, 17176, Sweden
    Recruiting
    • Jeffrey Yachnin · Principal investigator
  • University Hospital Birmingham
    Birmingham, United Kingdom
    Recruiting
    • Julia Scarisbrick, Prof. · Contact
  • University Hospitals of Leicester NHS Trust
    Leicester, LE1 5WW, United Kingdom
    Recruiting
    • Harriet Walter · Principal investigator
  • Guy's and Saint Thomas' NHS Foundation Trust
    London, SE1 9RT, United Kingdom
    Recruiting
    • Stephen Morris · Principal investigator
  • Sarah Cannon Research Institute UK
    London, W1G 6AD, United Kingdom
    Recruiting
    • Anja Williams · Principal investigator
  • The Royal Marsden Hospital NHS Foundation Trust
    London, United Kingdom
    Recruiting
    • Juanita Lopez · Principal investigator
  • The Christie NHS Foundation Trust
    Manchester, M20 4BX, United Kingdom
    Recruiting
    • Richard Cowan · Principal investigator
  • Southampton General Hospital
    Southampton, SO16 6YD, United Kingdom
    Recruiting
    • Sean Lim · Principal investigator
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking 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 Jan 2021 (actual). Primary completion is estimated for Jan 2028, 84 months after the start.

Of 116 industry-sponsored phase 1/2 interventional studies under Ovarian Neoplasms, half reached primary completion within 61 months of starting (the median), counting those still running; a quarter within 44 and three quarters within 88. This study's planned 84 months is above that.

Counting every sponsor, half of 173 studies reached it within 65 months; a quarter within 44 and three quarters within 100.

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

Registered
Dec 15, 2020
First posted
Feb 12, 2021
StartActual
Jan 25, 2021
Primary completionEst.
Jan 31, 2028
CompletionEst.
Dec 31, 2028
Last update
Sep 18, 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.
No changes since tracking began. The registry record was last updated on Sep 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04752826
Lead sponsor
BioInvent International AB
Responsible party
Sponsor
First posted
Feb 12, 2021
Start date
Jan 25, 2021
Primary completion
Jan 31, 2028 (estimated)
Completion
Dec 31, 2028 (estimated)
Last update
Sep 18, 2026

Study contacts

Susanne Gertsson
Contact
susanne.gertsson@bioinvent.com
+46462868550
Mona Welschof, PhD
Contact
mona.welschof@bioinvent.com
+47 97088721
Andres McAllister, PhD
study director · BioInvent International AB

Oversight

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

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