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Clinical Trial Finder

Search Results

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

Study Purpose

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.

Recruitment Criteria

Accepts Healthy Volunteers

Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms

No
Study Type

An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.


An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes.


Searching Both is inclusive of interventional and observational studies.

Interventional
Eligible Ages 18 Years and Over
Gender All
More Inclusion & Exclusion Criteria

Key

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.
Key

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 Details

Trial ID:

This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.

NCT04083599
Phase

Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans.

Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data.

Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.

Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.

Phase 1/Phase 2
Lead Sponsor

The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.

Genmab
Principal Investigator

The person who is responsible for the scientific and technical direction of the entire clinical study.

Study Official
Principal Investigator Affiliation Genmab
Agency Class

Category of organization(s) involved as sponsor (and collaborator) supporting the trial.

Industry
Overall Status Active, not recruiting
Countries Denmark, France, Georgia, Germany, Israel, Italy, Moldova, South Korea, Spain, Taiwan, United Kingdom, United States
Conditions

The disease, disorder, syndrome, illness, or injury that is being studied.

Malignant Solid Tumor, Non-Small Cell Lung Cancer (NSCLC), Colorectal Cancer (CRC), Melanoma, Head and Neck Squamous Cell Carcinoma (HNSCC), Pancreatic Ductal Adenocarcinoma (PDAC)
Additional Details

This is an open-label, multicenter phase 1/2 study designed to assess the safety, pharmacokinetics, pharmacodynamics and anti-tumor activity of GEN1042 administered as a monotherapy or in combination in participants with metastatic or locally advanced solid tumors. Participants will receive either GEN1042 alone, GEN1042 with pembrolizumab, or GEN1042 with pembrolizumab and chemotherapy. All participants will receive active drug; no one will receive placebo. This trial has 2 parts. The purpose of the first part is to find out if GEN1042 is safe and to find out the best doses of GEN1042 to use. The purpose of the second part is to give GEN1042 to more participants to see how well the dose(s) of GEN1042 selected in the first part work against cancer with GEN1042 when given alone or in combination with pembrolizumab or in combination with pembrolizumab and chemotherapy. Trial details include:

  • - The average trial duration will be about 3 years.
  • - The treatment duration will be up to 2 years (when GEN1042 is combined with pembrolizumab).
  • - The visit frequency will be weekly at first and lessening over time until visits are only once every 3 weeks.

Arms & Interventions

Arms

Experimental: Monotherapy - Dose Escalation and Dose Expansion Parts

Experimental: Combination Therapy - Safety Run-in and Expansion Parts

Interventions

Biological: - GEN1042

Intravenous

Drug: - Pembrolizumab

Intravenous

Drug: - Cisplatin

Intravenous

Drug: - Carboplatin

Intravenous

Drug: - 5-FU

Intravenous

Drug: - Gemcitabine

Intravenous

Drug: - Nab paclitaxel

Intravenous

Drug: - Pemetrexed

Intravenous

Drug: - Paclitaxel

Intravenous

Contact a Trial Team

If you are interested in learning more about this trial, find the trial site nearest to your location and contact the site coordinator via email or phone. We also strongly recommend that you consult with your healthcare provider about the trials that may interest you and refer to our terms of service below.

Alaska Oncology and Hematology LLC, Anchorage 5879400, Alaska 5879092

Status

Address

Alaska Oncology and Hematology LLC

Anchorage 5879400, Alaska 5879092, 99508

Cancer & Blood Specialty Clinic, Los Alamitos 5368304, California 5332921

Status

Address

Cancer & Blood Specialty Clinic

Los Alamitos 5368304, California 5332921, 90720

San Diego 5391811, California 5332921

Status

Address

Moores Cancer Center at the UC San Diego Health

San Diego 5391811, California 5332921, 92037

Yale University Cancer Center, New Haven 4839366, Connecticut 4831725

Status

Address

Yale University Cancer Center

New Haven 4839366, Connecticut 4831725, 06520

ChristianaCare, Newark 4143861, Delaware 4142224

Status

Address

ChristianaCare

Newark 4143861, Delaware 4142224, 19713

Mount Sinai Comprehensive Cancer Center, Miami Beach 4164143, Florida 4155751

Status

Address

Mount Sinai Comprehensive Cancer Center

Miami Beach 4164143, Florida 4155751, 33140

Florida Cancer Affiliates, Ocala 4166673, Florida 4155751

Status

Address

Florida Cancer Affiliates

Ocala 4166673, Florida 4155751, 34474

Hope and Healing Cancer Services, Hinsdale 4896012, Illinois 4896861

Status

Address

Hope and Healing Cancer Services

Hinsdale 4896012, Illinois 4896861, 60521

University of Kentucky, Lexington 4297983, Kentucky 6254925

Status

Address

University of Kentucky

Lexington 4297983, Kentucky 6254925, 40536

Norton Cancer Institute, Louisville 4299276, Kentucky 6254925

Status

Address

Norton Cancer Institute

Louisville 4299276, Kentucky 6254925, 40202

Maryland Oncology Hematology PA, Columbia 4352053, Maryland 4361885

Status

Address

Maryland Oncology Hematology PA

Columbia 4352053, Maryland 4361885, 21044

Washington University School of Medicine, St Louis 4407066, Missouri 4398678

Status

Address

Washington University School of Medicine

St Louis 4407066, Missouri 4398678, 63110

Levine Cancer Center, Charlotte 4460243, North Carolina 4482348

Status

Address

Levine Cancer Center

Charlotte 4460243, North Carolina 4482348, 28204

Winston-Salem 4499612, North Carolina 4482348

Status

Address

Novant Health Cancer Institute - Forsyth (Medical Oncology)

Winston-Salem 4499612, North Carolina 4482348, 27103

Portland 5746545, Oregon 5744337

Status

Address

Kaiser Permanente (KP) Oncology/Hematology

Portland 5746545, Oregon 5744337, 97227

University of Pennsylvania, Philadelphia 4560349, Pennsylvania 6254927

Status

Address

University of Pennsylvania

Philadelphia 4560349, Pennsylvania 6254927, 19104

Fox Chase Cancer Center, Philadelphia 4560349, Pennsylvania 6254927

Status

Address

Fox Chase Cancer Center

Philadelphia 4560349, Pennsylvania 6254927, 19111

Sarah Cannon Research Institute, Nashville 4644585, Tennessee 4662168

Status

Address

Sarah Cannon Research Institute

Nashville 4644585, Tennessee 4662168, 37203

Lumi Research, Kingwood 7534469, Texas 4736286

Status

Address

Lumi Research

Kingwood 7534469, Texas 4736286, 77339

Utah Cancer Specialists, Salt Lake City 5780993, Utah 5549030

Status

Address

Utah Cancer Specialists

Salt Lake City 5780993, Utah 5549030, 84124

Virgina Cancer Specialists, Fairfax 4758023, Virginia 6254928

Status

Address

Virgina Cancer Specialists

Fairfax 4758023, Virginia 6254928, 22031

Adventist Health System/Sunbelt,Inc, Seattle 5809844, Washington 5815135

Status

Address

Adventist Health System/Sunbelt,Inc

Seattle 5809844, Washington 5815135, 98109

Medical Oncology Associates, PS, Spokane 5811696, Washington 5815135

Status

Address

Medical Oncology Associates, PS

Spokane 5811696, Washington 5815135, 99204

International Sites

Copenhagen 2618425, Denmark

Status

Address

Rigshospitalet (Copenhagen University Hospital)

Copenhagen 2618425, ,

Herlev University Hospital, Herlev 2620431, Denmark

Status

Address

Herlev University Hospital

Herlev 2620431, ,

Vejle 2610613, Denmark

Status

Address

University Hospital of Southern Denmark, Vejle Hospital

Vejle 2610613, ,

Bordeaux 3031582, France

Status

Address

Centre hospitalier Universitaire de Bordeaux

Bordeaux 3031582, ,

Centre Antoine Lacassagne, Nice 2990440, France

Status

Address

Centre Antoine Lacassagne

Nice 2990440, ,

Gustave Roussy, Villejuif 2968705, France

Status

Address

Gustave Roussy

Villejuif 2968705, ,

Tbilisi 611717, Georgia

Status

Address

ARENSIA Research Clinic at the Research Institute of Clinical Medicine

Tbilisi 611717, ,

Heidelberg 2907911, Germany

Status

Address

Nationales Centrum fr Tumorerkrankungen NCT

Heidelberg 2907911, ,

Ludwigshafen 2875377, Germany

Status

Address

Klinikum der Stadt Ludwigshafen am Rhein gGmbH

Ludwigshafen 2875377, ,

Mainz 2874225, Germany

Status

Address

Department of Dermatology, University of Mainz

Mainz 2874225, ,

Mannheim 2873891, Germany

Status

Address

Universitätsmedizin Mannheim Dermatologie

Mannheim 2873891, ,

Universitaetsklinikum Wuerzburg, Würzburg 2805615, Germany

Status

Address

Universitaetsklinikum Wuerzburg

Würzburg 2805615, ,

Rabin Medical Center, Petah Tikva 293918, Israel

Status

Address

Rabin Medical Center

Petah Tikva 293918, ,

Tel Aviv Sourasky Medical Center, Tel Aviv 293397, Israel

Status

Address

Tel Aviv Sourasky Medical Center

Tel Aviv 293397, ,

Brescia 3181554, Italy

Status

Address

Azienda Ospedaliera Spedali Civili di Brescia

Brescia 3181554, ,

Cuneo 3177700, Italy

Status

Address

Azienda Ospedaliera S.Croce e Carle Cuneo

Cuneo 3177700, ,

Istituto Nazionale dei Tumori, Milan 3173435, Italy

Status

Address

Istituto Nazionale dei Tumori

Milan 3173435, ,

Istituto Clinico Humanitas, Rozzano 3168837, Italy

Status

Address

Istituto Clinico Humanitas

Rozzano 3168837, ,

Chisinau 618426, Moldova

Status

Address

ARENSIA Research Clinic at the Oncology Institute

Chisinau 618426, ,

Chungbuk National University Hospital, Cheongju-si 1845604, South Korea

Status

Address

Chungbuk National University Hospital

Cheongju-si 1845604, ,

Jeonbuk National University Hospital, Jeonju 1845457, South Korea

Status

Address

Jeonbuk National University Hospital

Jeonju 1845457, ,

Gachon University Gil Medical Center, Namdong 11169442, South Korea

Status

Address

Gachon University Gil Medical Center

Namdong 11169442, ,

Korea University Guro Hospital, Seoul 1835848, South Korea

Status

Address

Korea University Guro Hospital

Seoul 1835848, ,

Samsung Medical Center, Seoul 1835848, South Korea

Status

Address

Samsung Medical Center

Seoul 1835848, ,

Seoul 1835848, South Korea

Status

Address

Severance Hospital, Yonsei University Health System

Seoul 1835848, ,

Yangsan 1832828, South Korea

Status

Address

Pusan National University Yangsan Hospital

Yangsan 1832828, ,

H. Vall d'Hebron, Barcelona 3128760, Spain

Status

Address

H. Vall d'Hebron

Barcelona 3128760, ,

START Barcelona HM Nou Delfos, Barcelona 3128760, Spain

Status

Address

START Barcelona HM Nou Delfos

Barcelona 3128760, ,

L'Hospitalet de Llobregat 3120619, Spain

Status

Address

Hospital Duran i Reynals - ICO L Hospitalet

L'Hospitalet de Llobregat 3120619, ,

Las Palmas de Gran Canaria 2515270, Spain

Status

Address

Hospital Universitario Insular de Gran Canaria

Las Palmas de Gran Canaria 2515270, , 35016

Hospital Universitario Lucus Augusti, Lugo 3117814, Spain

Status

Address

Hospital Universitario Lucus Augusti

Lugo 3117814, ,

Clinica Universidad de Navarra, Madrid 3117735, Spain

Status

Address

Clinica Universidad de Navarra

Madrid 3117735, ,

Madrid 3117735, Spain

Status

Address

HM CIOCC Hospital Universitario HM Sanchinarro

Madrid 3117735, ,

Hospital Clinico San Carlos, Madrid 3117735, Spain

Status

Address

Hospital Clinico San Carlos

Madrid 3117735, ,

Madrid 3117735, Spain

Status

Address

Hospital General Universitario Gregorio Maran

Madrid 3117735, ,

Hospital Universitario 12 de Octubre, Madrid 3117735, Spain

Status

Address

Hospital Universitario 12 de Octubre

Madrid 3117735, ,

Hospital Universitario La Paz, Madrid 3117735, Spain

Status

Address

Hospital Universitario La Paz

Madrid 3117735, ,

Hospital Universitario Ramon y Cajal, Madrid 3117735, Spain

Status

Address

Hospital Universitario Ramon y Cajal

Madrid 3117735, ,

MD Anderson Cancer Center Madrid, Madrid 3117735, Spain

Status

Address

MD Anderson Cancer Center Madrid

Madrid 3117735, ,

Madrid 3117735, Spain

Status

Address

START Madrid - Hospital Universitario Fundacion Jimenez Diaz

Madrid 3117735, ,

Málaga 2514256, Spain

Status

Address

Hospital Universitario Virgen de la Victoria

Málaga 2514256, ,

Clinica Universidad de Navarra, Pamplona 3114472, Spain

Status

Address

Clinica Universidad de Navarra

Pamplona 3114472, ,

Santiago de Compostela 3109642, Spain

Status

Address

Complejo Hospitalario Universitario de Santiago (CHUS)

Santiago de Compostela 3109642, ,

Hospital Virgen del Rocio, Seville 2510911, Spain

Status

Address

Hospital Virgen del Rocio

Seville 2510911, ,

Valencia 2509954, Spain

Status

Address

Hospital Clinico Universitario de Valencia

Valencia 2509954, ,

Kaohsiung City 1673820, Taiwan

Status

Address

Chang Gung Memorial Hospital (CGMH) - Kaohsiung Branch

Kaohsiung City 1673820, ,

Kaohsiung City 1673820, Taiwan

Status

Address

Kaohsiung Medical University Memorial Hospital

Kaohsiung City 1673820, ,

China Medical University Hospital, Taichung 1668399, Taiwan

Status

Address

China Medical University Hospital

Taichung 1668399, ,

National Cheng Kung University Hospital, Tainan City 1668355, Taiwan

Status

Address

National Cheng Kung University Hospital

Tainan City 1668355, ,

Taipei Medical University Hospital, Taipei 1668341, Taiwan

Status

Address

Taipei Medical University Hospital

Taipei 1668341, ,

Taipei Veterans General Hospital, VGHTPE, Taipei 1668341, Taiwan

Status

Address

Taipei Veterans General Hospital, VGHTPE

Taipei 1668341, ,

Taoyuan District 1667905, Taiwan

Status

Address

Chang Gung Memorial Hospital Linkou Branch

Taoyuan District 1667905, ,

Royal Marsden NHS Foundation Trust, Sutton 2636503, United Kingdom

Status

Address

Royal Marsden NHS Foundation Trust

Sutton 2636503, ,

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