GEN1042 Safety Trial and Anti‑tumor Activity in Participants With Malignant Solid Tumors

Trial status:Recruitment Complete
Trial ID:
GCT1042-01
NCT ID:
NCT04083599
EudraCT ID:
2018-003716-47
EU Trial (CTIS) Number:
2023-508526-10
Sponsor:
The sponsor of a clinical trial is the company, institution or individual that takes responsibility for initiating, managing, and/or financing a clinical investigation. BioNTech collaborates with other pharmaceutical companies or institutions (collaborators) to develop certain new medicines. In particular cases BioNTech's collaborators are leading specific clinical trials and are acting as sponsors accordingly.
Genmab
Recruitment Complete

Trial Details

The goal of this trial is to learn about the antibody GEN1042 when it is used alone and when it is used together with another antibody cancer drug, pembrolizumab (with or without chemotherapy), for treatment of participants with certain types of cancer.

Medical Condition
  • Solid Tumors
  • Lung Cancer
  • Colorectal Cancer
  • Skin Cancer
  • Head and Neck Cancer
  • Pancreatic Cancer
    • Trial Drug
  • GEN1042
    • See more
  • Pembrolizumab
  • Cisplatin
  • Carboplatin
  • 5-FU
  • Gemcitabine
  • Nab paclitaxel
  • Pemetrexed
  • Paclitaxel
    • Phase
    Phase 1/Phase 2
    Type
    Interventional
    Estimated Enrolment
    1287
    Estimated Trial Date
    Sep 2019 - Dec 2025

    Trial Participant Requirements

    Age
    18+ years
    Sex
    Female & Male
    Healthy Volunteers
    No
    Inclusion and Exclusion Criteria
    Inclusion criteria

      Monotherapy - Dose Escalation and Dose Expansion Parts

    • Participants with non-CNS solid tumors that is metastatic or unresectable and for whom there is no available standard therapy.
    • Participants with a confirmed diagnosis of relapsed or refractory, advanced and/or metastatic melanoma, NSCLC, or CRC and for whom there is no available standard therapy

      • Combination Therapy - Dose Expansion Part

    • Participants with unresectable Stage III or Stage IV melanoma with no prior systemic anticancer therapy for unresectable or metastatic disease. Primary ocular or mucosal melanoma is excluded.
    • Participants with Stage IV metastatic or recurrent NSCLC with no prior systemic anticancer therapy, no actionable mutation.
    • Participants with recurrent or metastatic HNSCC with no prior systemic therapy administered in the recurrent or metastatic setting.
    • Participants with confirmed metastatic PDAC with no previous radiotherapy, surgery, chemotherapy, or investigational therapy for the treatment of metastatic disease.

      • General (all phases):

    • Must be age ≥ 18 years of age on the day of signing informed consent, or the legal age of consent in the jurisdiction in which the trial is taking place.
    • Measurable disease according to RECIST 1.1
    • Eastern Cooperative Oncology Group (ECOG) 0-1
    • Normal or adequate liver, renal, cardiac and bone marrow function
    Exclusion criteria

      Monotherapy - Dose Escalation and Dose Expansion Parts

    • Treatment with an anti-cancer agent (within 21 days or after at least 5 half-lives of the drug, whichever is shorter), prior to GEN1042 administration
    • Radiotherapy within 14 days prior to first GEN1042 administration
    • Toxicities from previous anti-cancer therapies that have not resolved

      • Combination Therapy - Dose Expansion Part

    • Has received prior systemic cytotoxic chemotherapy, biological therapy, OR major surgery within 3 weeks or at least 5 half-lives of the drug (whichever is shorter) of the first dose of trial treatment.
    • Radiotherapy within 14 days of start of trial treatment or received lung radiation therapy of \> 30 Gy within 6 months of the first dose of trial treatment.

      • General (all phases)

    • Participants has an active, known, or suspected autoimmune disease.
    • History of non-infectious pneumonitis that required steroids or currently has pneumonitis.
    • History of ≥ grade 3 allergic reactions to monoclonal antibody (mAb) therapy
    • Participants with a condition requiring systemic treatment with either corticosteroids (\>10 mg daily prednisone equivalent) or other immunosuppressive medications within 14 days of first treatment.

      • NOTE: Other protocol defined Inclusion/Exclusion criteria may apply.

    Trial Locations

    Location
    Status
    Location
    Alaska Oncology and Hematology LLC
    Anchorage, Alaska, United States, 99508
    Status
    Location
    Cancer & Blood Specialty Clinic
    Los Alamitos, California, United States, 90720
    Status
    Location
    Moores Cancer Center at the UC San Diego Health
    San Diego, California, United States, 92037
    Status
    Location
    Yale University Cancer Center
    New Haven, Connecticut, United States, 06520
    Status
    Location
    ChristianaCare
    Newark, Delaware, United States, 19713
    Status
    Location
    Mount Sinai Comprehensive Cancer Center
    Miami Beach, Florida, United States, 33140
    Status
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