Ifinatamab Deruxtecan (I-DXd): I-DXd will be administered as an intravenous (IV) infusion on Day 1 of each 21-day cycle (every Q3W).
Study summary
This 2-part study intends to define the recommended Phase 2 dose of ifinatamab deruxtecan (I-DXd) based on the efficacy, safety, and pharmacokinetics (PK) results observed in participants with Extensive-stage Small Cell Lung Cancer (ES-SCLC) who received at least 1 prior line of platinum-based chemotherapy and a maximum of 3 prior lines of therapy (Part 1) and a minimum of two previous lines of systemic therapy (Part 2). This study will also investigate I-DXd anti-tumor activity in this population.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
Participants must meet all the following criteria to be eligible for enrollment into the study:
* Sign and date the informed consent form (ICF) prior to the start of any study-specific qualification procedures.
* Participant must have at least one lesion, not previously irradiated, amenable to core biopsy.
* Male or female subjects aged ≥18 years (follow local regulatory requirements if the legal age of consent for study participation is \>18 years old).
* Histologically or cytologically documented ES-SCLC.
* At least one measurable lesion according to RECIST v1.1 as assessed by the investigator.
* Prior therapy with at least one platinum-based line as systemic therapy for extensive-stage disease with at least two cycles of therapy (except in the case of early objective PD) and beginning with protocol version 3.0, a minimum of two previous lines of systemic therapy.
* Documentation of radiological disease progression on or after most recent systemic therapy.
* Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1.
Exclusion Criteria:
Participants who meet any of the following criteria will be disqualified from entering the study:
* Prior treatment with orlotamab, enoblituzumab, or other B7-H3 targeted agents, including I-DXd.
* Prior discontinuation of an antibody drug conjugate (ADC) that consists of an exatecan derivative (eg, trastuzumab deruxtecan) due to treatment-related toxicities.
* Clinically active brain metastases, spinal cord compression or leptomeningeal carcinomatosis, defined as untreated or symptomatic, or requiring therapy with steroids or anticonvulsants to control associated symptoms.
* Any of the following conditions within the past 6 months: cerebrovascular accident, transient ischemic attack, or another arterial thromboembolic event.
* Clinically significant corneal disease.
* Uncontrolled or significant cardiovascular disease.
* History of (non-infectious) interstitial lung disease (ILD)/pneumonitis that required corticosteroids, current ILD/pneumonitis, or suspected ILD/pneumonitis that cannot be ruled out by imaging at screening.
* Clinically severe pulmonary compromise resulting from intercurrent pulmonary illnesses,
* Chronic steroid treatment (dose of 10 mg daily or more prednisone equivalent), except for low-dose inhaled steroids (for asthma/COPD) or topical steroids (for mild skin conditions) or intra-articular steroid injections.
* History of malignancy other than SCLC within the 3 years prior to enrollment, except adequately resected non-melanoma skin cancer, curatively treated in situ disease, superficial gastrointestinal (GI) tract tumors and non-muscle invasive bladder cancer curatively resected by endoscopic surgery.
* History of allogeneic bone marrow, stem cell, or solid organ transplant.
* Unresolved toxicities from previous anticancer therapy, defined as toxicities (other than alopecia) not yet resolved to National Cancer Institute- Common Terminology Criteria for Adverse Events Version 5.0 (NCI-CTCAE V5.0), Grade ≤1 or baseline.
* History of hypersensitivity to the drug substances, inactive ingredients in the drug product or severe hypersensitivity reactions to other monoclonal antibodies.
* Evidence of ongoing uncontrolled systemic bacterial, fungal, or viral infection.
* Has active or uncontrolled hepatitis B or C infection.
* Active, known, or suspected autoimmune disease.
* Any evidence of severe or uncontrolled systemic diseases (including active bleeding diatheses, psychiatric illness/social situations, substance abuse).
* Has received a live vaccine within 30 days prior to the first dose of study drug.
* Female who is pregnant or breast-feeding or intends to become pregnant during the study.
* Prior or ongoing clinically relevant illness, medical condition, surgical history, physical finding, or laboratory abnormality that, in the investigator's opinion, could affect the safety of the participant.
* Known human immunodeficiency virus (HIV) infection that is not well controlled.
Primary outcome measure(s)
Percentage of Participants With Objective Response Rate (ORR) Based on Blinded Independent Central Review (BICR) Following Treatment With I-DXd in Participants With Pretreated ES-SCLC — Up to approximately 36 months ORR was defined as the percentage of participants who achieved a best overall response (BOR) of confirmed Complete Response (CR) or Partial Response (PR), assessed by BICR based on RECIST version 1.1. For all target, non-target, and new lesions, CR was defined as a disappearance of all lesions and PR was defined as at least a 30% decrease in the sum of diameters of all lesions.
Trial sites (58)
Facility
City
Region
Status
Highlands Oncology Group
Springdale
Arkansas
The Cancer Specialists, Llc
Jacksonville
Florida
H. Lee Moffitt Cancer Center and Research Institute
Tampa
Florida
University of Chicago Medical Center
Chicago
Illinois
Johns Hopkins Sidney Kimmel Comprehensive Cancer Center
Baltimore
Maryland
Dana-Faeber Cancer Institute
Boston
Massachusetts
Henry Ford Hospital
Detroit
Michigan
Cancer and Hematology Centers of Western Michigan
Grand Rapids
Michigan
Washington University School of Medicine
St Louis
Missouri
Hackensack Meridian Health-Southern Ocean Medical Center
Manahawkin
New Jersey
Memorial Sloan-Kettering Cancer Center (Mskcc) - New York
New York
New York
Montefiore Medical Center Prime
The Bronx
New York
Duke University Health System
Durham
North Carolina
Sarah Cannon (Tennessee Oncology - Nashville)
Nashville
Tennessee
Millennium Physicians Association, Llp
Houston
Texas
University of Washington Medical Center
Seattle
Washington
Jilin Cancer Hospital
Changchun
China
Hunan Cancer Hospital
Changsha
China
West China Hospital, Sichuan University
Chengdu
China
Guangdong Provincial People'S Hospital
Guangdong
China
Zhejiang Cancer Hospital
Hangzhou
China
Linyi Cancer Hospital
Linyi
China
Fudan University Shanghai Cancer Center
Shanghai
China
Union Hospital of Tongji Medical College Huazhong University of Science and Technology
Wuhan
China
Centre Hospitalier Intercommunal de Créteil
Créteil
France
Centre Leon Berard
Lyon
France
Hôpital Nord - Chu Marseille
Marseille
France
CHU de Montpellier - Hôpital Arnaud de Villeneuve
Montpellier
France
Hopital Arnaud de Villeneuve
Montpellier
France
Institut Curie - Site de Paris
Paris
France
Hopital Tenon
Paris
France
Evangelische Lungenklinik Berlin
Berlin
Germany
Universitaetsklinikum Essen
Essen
Germany
National Cancer Center Hospital
Chūōku
Japan
National Cancer Center Hospital East
Kashiwa
Japan
The Cancer Institute Hospital of Jfcr
Kōtoku
Japan
Shizuoka Cancer Center
Nagaizumi-chō
Japan
Osaka International Cancer Institute
Osaka
Japan
Kindai University Hospital
Ōsaka-sayama
Japan
Kanagawa Cancer Center
Yokohama
Japan
+ 18 more sites — see the full list on the official registry below.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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