Study to Assess AFM24 in Combination With Atezolizumab in Selected Advanced/Metastatic EGFR-expressing Cancers

NCT ID: NCT05109442

Last Updated: 2025-08-20

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 112 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-11-19
• Study Completion Date: 2025-06-11

Brief Summary

AFM24-102 is a Phase 1/2a open-label, non-randomized, multicenter, dose escalation, and expansion study evaluating AFM24 in combination with atezolizumab in patients with selected EGRF-expressing advanced solid malignancies whose disease has progressed after treatment with previous anticancer therapies.

Detailed Description

There will be 2 parts in this study: a dose escalation phase (phase 1) and an expansion phase (phase 2a). Patients will qualify to receive the investigational drugs (AFM24 + atezolizumab) in the dose escalation phase or the expansion phase only if they are deemed eligible following the safety lead-in phase. Seven days before the planned first combination treatment, patients will receive a single dose of AFM24 and will be observed for any adverse events for 1 week.

The aim of the dose escalation phase is to determine the maximum tolerated dose (MTD)/recommended phase 2 dose (RP2D) of AFM24 in combination with atezolizumab.

The dose escalation phase will be followed by the expansion phase once the MTD/RP2D of AFM24 in combination with atezolizumab has been determined. The expansion phase of the study is intended to collect preliminary evidence of efficacy and to further confirm the safety of AFM24 in combination with atezolizumab.

The tumor types planned to be studied in the AFM24/atezolizumab combination study will be:

• Non-small cell lung cancer (EGFR-WT), with disease progression after chemotherapy and PD1/PD-L1 targeted therapy
• Gastric/GEJ cancer if intolerant to or with disease progression after standard platinum-based chemotherapy
• Pancreatic/hepatocellular/biliary tract cancer with disease progression after standard of care (SOC) therapy or if there is no appropriate SOC available for their condition
• Advanced or metastatic NSCLC harboring a targetable EGFR kinase domain mutation with disease progression on or after received ≥1 prior lines of treatment for advanced disease, including a Tyrosine-Kinase Inhibitor (TKI) for EGFR mutations

Conditions

Advanced Solid Tumor

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Escalation Phase

The Escalation phase will determine the MTD/RP2D of AFM24 in combination with atezolizumab. A traditional 3+3 design will be used to determine the RP2D.

Group Type: EXPERIMENTAL

AFM24

Intervention Type: DRUG

intravenous infusion

Atezolizumab 840 MG in 14 ML Injection

Intervention Type: DRUG

intravenous infusion

Expansion Phase

The expansion phase will collect preliminary evidence of efficacy and further confirm the safety of AFM24 in combination with atezolizumab.

Group Type: EXPERIMENTAL

AFM24

Intervention Type: DRUG

intravenous infusion

Atezolizumab 840 MG in 14 ML Injection

Intervention Type: DRUG

intravenous infusion

Interventions

AFM24

intravenous infusion

Intervention Type: DRUG

Atezolizumab 840 MG in 14 ML Injection

intravenous infusion

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Histologically or cytologically confirmed advanced or metastatic EGFR-positive selected cancer types (except for NSCLC)
• Advanced or metastatic NSCLC, EGFR WT: disease has progressed after ≥ 1 prior lines of therapy which must have included a platinum-based doublet in combination with PD1/PD-L1 antibody or must have received an anti-PD1/PD-L1 antibody prior to or after a platinum-based doublet
• Advanced, unresectable, or metastatic gastric/GEJ adenocarinoma: after ≥ 1 prior chemotherapy regimen including a platinum and fluoropyrimidine doublet
• Advanced or metastatic HCC (BCLC C or B not amenable or refractory to locoregional therapy), hepatobiliary-, or pancreatic adenocarcinoma: after ≥1 prior line of an approved SOC therapy for the respective disease type or to whom the available SOC is not appropriate in the opinion of the investigator
• Advanced or metastatic NSCLC harboring a targetable EGFR kinase domain mutation and whose disease has progressed on or after having received ≥ prior TKI approved for EGFR mutated NSCLC. Subjects treated with a 1st or 2nd generation TKI in 1st line who developed a documented T790M mutation must have received a TKI targeting this mutation such as Osimertinib or Lazertinib to be eligible. Subjects must have documentation of EGFR mutated NSCLC as assessed by an approved test using genomic sequencing of tumor or circulation free tumor DNA. The patients should have received a 2nd line of treatment if approved and available or may be enrolled in the study if in the opinion of the investigator it is in the patient's best interest,or the SOC is not appropriate.
• Adequate organ function
• Phase 1: Evaluable or measurable disease per RECIST v1.1
• Phase 2a: Measurable disease per RECIST v1.1

Exclusion Criteria

• Treatment with systemic anticancer therapy including investigational agent within 4 weeks of the first dose of study drug, 6 weeks for mitomycin C or nitrosoureas, 2 weeks (or 5 half-lives whichever is longer) for using fluorouracil or small molecule targeted drugs, 2 weeks for using traditional Chinese medicine with anti-tumor indication.
• Radiation therapy within 2 weeks before 1st dose of study drug or unresolved toxicity from previous radiotherapy
• History of any other malignancy known to be active, with the exception of completely removed in situ cervical intra-epithelial neoplasia, non-melanoma skin cancer, DCIS, early stage prostate cancer that has been adequately treated, and other cancers from which the patient has been disease free for 3 years or longer
• Currently active in any other clinical study, or administration of other investigational agent

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Affimed GmbH

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Daniela Morales-Espinosa, MD

Role: STUDY_DIRECTOR

Affimed GmbH

Locations

USC Norris Comprehensive Cancer Center

Los Angeles, California, United States

University of Chicago Medical Center

Chicago, Illinois, United States

Johns Hopkins University

Baltimore, Maryland, United States

Independent Public Teaching Hospital #4 in Lublin, Department of Clinical Oncology and Chemotherapy

Lublin, , Poland

European Health Center Otwock Fryderyk Chopin Hospital, Department of Clinical Oncology

Otwock, , Poland

MED-Polonia, Sp. z o.o. (LLC)

Poznan, , Poland

Janusz Korczak Provincial Specialist Hospital in Slupsk Limited Liability Company

Słupsk, , Poland

Maria Sklodowska-Curie - National Research Institute of Oncology, Early Phase Research Department

Warsaw, , Poland

Seoul National University Bundang Hospital

Seongnam-si, , South Korea

Severance Hospital, Yonsei University Health System

Seoul, , South Korea

The Catholic University of Korea St. Vincent's Hospital

Suwon, , South Korea

Vall d'Hebron Institute of Oncology (VHIO)

Barcelona, , Spain

University Hospital Quiron Madrid

Madrid, , Spain

University Clinic of Navarra - Pamplona

Pamplona, , Spain

Hospital Clinic Universitario Biomedical Research institute INCLIVA

Valencia, , Spain

Royal Marsden NHS Foundation Trust - ICR

Sutton, , United Kingdom

Countries

United States; Poland; South Korea; Spain; United Kingdom

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

AFM24-102

Identifier Type: -

Identifier Source: org_study_id