GEN1047 for Solid Tumors - First in Human (FIH) Trial

Phase 2TerminatedNCT05180474

Genmab179 enrolled

Overview

The purpose of this trial is to measure the following in participants with solid tumors who receive GEN1047: * The side effects seen with GEN1047 * What the body does with GEN1047 once it is administered * What GEN1047 does to the body once it is administered * How well GEN1047 works against solid tumors The estimated trial duration for an individual participant is 8 months, consisting of a 28-day screening period, an estimated 3 month treatment period (the duration of treatment may vary for each participant), and an estimated 4 month post-treatment follow-up period (the duration of follow-up may vary for each participant). All participants will receive active drug; no one will be given placebo.

The trial is an open-label, multi-center safety trial of GEN1047. The trial consists of two parts: a dose escalation part ("escalation" - phase 1) and an expansion part ("expansion" - phase 2a). The goal of the dose escalation part is to find out if GEN1047 is safe in participants with specific solid tumors and to find the best dose(s). In the expansion part of the trial up to two doses of GEN1047 will be tested.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

179

Conditions

Breast Cancer, Breast Neoplasms Endometrial Cancer, Endometrial Neoplasm

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Key Inclusion Criteria: Criteria - Escalation Part: * Participant must have histologically or cytologically confirmed solid tumor(s) in any of the following selected indications for which there is no further available standard therapy likely to confer clinical benefit (or participant is not a candidate or has previously refused such earlier available therapy), and for whom, in the opinion of the investigator, experimental therapy with GEN1047 may be beneficial (breast cancer, endometrial cancer, ovarian cancer, NSCLC-SCC. * Participants with ovarian cancer must have documented progressive disease (PD) on or after last prior treatment and within 60 days of screening. * Must be at least 18 years of age (or the legal age of consent in the jurisdiction in which the trial is taking place) on the day of signing informed consent. * Must have either recurrence after, or progression on or lack of response to available relevant standard of care (SoC) anticancer therapies; or are deemed intolerant to or ineligible for, standard curative therapy in the recurrent setting. * Must have at least 1 measurable lesion per RECIST v1.1. The measurable lesion(s) must be outside the field of radiation therapy (RT) if there was prior treatment with RT. * Must have an Eastern Cooperative Oncology Group performance status (ECOGPS) score of 0 to 1 at Screening and on C1D1 pretreatment. * Should provide a tumor tissue sample during the Screening period and prior to C1D1. * Provide all tumor-assessing pre-trial CT scans since failure of last prior therapy. Criteria - Expansion Part Stage 1, 1b and Stage 2: * Participants must have documented PD according to RECIST v1.1 on or after last prior treatment with latest scan performed a maximum of 28 days prior to the first dose. * Participant must have advanced (unresectable) or metastatic, histologically confirmed diagnosis (breast cancer, endometrial cancer, ovarian cancer. * Must be a female and at least 18 years of age (or the legal age of consent in the jurisdiction in which the trial is taking place) at the time of consent. * Must have at least 1 measurable lesion per RECIST v1.1 as assessed by local investigator. * Must have an ECOG- PS score of 0 to 1 at Screening and on Cycle 1 Day 1 (C1D1) pretreatment. * Must submit a tumor tissue sample during the Screening period and prior to C1D1. * Provide all tumor-assessing pre-trial CT scans since failure of last prior therapy. Key Exclusion Criteria: * Significant cardiovascular impairment within 6 months of the first dose of trial drug. * Participant with new or progressive brain metastases or spinal cord compression. * Participant has been exposed to any prior therapy with a compound targeting CD3 and/or B7H4 or cell based therapies. * Current pneumonitis (any grade) including any radiological change of ongoing pneumonitis at baseline or history of non-infectious drug-, immune-, or radiation-related pneumonitis that required steroid. Note: Other protocol defined inclusion and exclusion criteria may apply.

Locations (36)

UCLA Department of Medicine Hematology Oncology

Los Angeles, California, United States

Yale University - Yale Cancer Center

New Haven, Connecticut, United States

Barbara Ann Karmanos Cancer Institute

Detroit, Michigan, United States

Case Western Reserve University

Cleveland, Ohio, United States

University of Pennsylvania

Philadelphia, Pennsylvania, United States

Outcomes

Primary Outcomes

Escalation: Number of Participants with Dose Limiting Toxicities (DLT)

DLTs will be graded for severity according to the National Cancer Institute-Common Terminology Criteria for Adverse Events (NCI-CTCAE), v5.0.

Time frame: From the first Cycle (Cycle length=21 days) in each cohort

Escalation: Number of Participants with Treatment Emergent Adverse Events (TEAEs)

An AE is any untoward medical occurrence in a participant or clinical investigation participant administered a pharmaceutical product and that does not necessarily have a causal relationship with this treatment. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal (investigational) product, whether or not related to the medicinal (investigational) product. TEAE is defined as an AE occurring or worsening between the first dose of study drug and 30 days after the last dose received.

Time frame: From first dose date up to end of the safety follow up period, 30 days after last dose (approximately 4 months)

Expansion: Objective Response Rate (ORR)

ORR is defined as percentage of participants with best overall response (BOR) of confirmed complete response (CR) or confirmed partial response (PR) based on RECIST v1.1.

Time frame: Up to 5 years