Study of Ifinatamab Deruxtecan (DS-7300a, I-DXd) in Participants With Advanced Solid Malignant Tumors

Recruiting now · Phase 1/Phase 2

Conditions studied: Advanced Solid Tumor, Malignant Solid Tumor

In brief

This is a single group study of participants with advanced solid tumors who have not been cured by other treatments. It is the first time the drug will be used in humans, and will be in two parts. The primary purpose of the parts are: * Dose Escalation Part: To evaluate the safety and tolerability and to determine the maximum tolerated dose and the recommended dose for expansion of ifinatamab deruxtecan (I-DXd). * Dose Expansion Part: To investigate the safety, tolerability and antitumor activity of I-DXd when administered as a single agent. This study is expected to last approximately 5 years from the time the first participant is enrolled to the time the last participant is off the study. The number of treatment cycles is not fixed in this study. Participants who continue to benefit from the study treatment may continue, unless: * they withdraw * their disease gets worse * they experience unacceptable side effects.

Key facts

Study ID

NCT04145622

Run by

Daiichi Sankyo

People needed

250

Starts

2019-11-03

Expected to finish

2029-10-31

Last updated by the study team

2026-05-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0 or 1.
• Has at least 1 measurable lesion according to Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 on computed tomography (CT) or magnetic resonance imaging (MRI) as assessed by Investigator. Measurable lesions should not be from a previously irradiated site. If the lesion at a previously irradiated site is the only selectable target lesion, a radiological assessment showing significant progression of the irradiated lesion should be provided by the Investigator
• Has adequate cardiac, hematopoietic, renal and hepatic functions
• Has an adequate treatment washout period prior to start of study treatment
• Has a pathologically documented advanced/unresectable or metastatic head and neck squamous cell carcinoma, esophageal squamous cell carcinoma, squamous and adenocarcinoma non-small cell lung cancer (NSCLC), small cell lung cancer (SCLC), bladder cancer, sarcoma, endometrial cancer, melanoma, adenocarcinoma CRPC (primary neuroendocrine or histologically confirmed neuroendocrine differentiated prostate cancer is not allowed), breast cancer that is refractory to or intolerable with standard treatment, or for which no standard treatment is available.
• For Expansion Cohort 4 2L ESCC participants only:
• Has disease progression a post platinum-based and an immune checkpoint inhibitor (ICI) treatment per global or local guidelines, with a maximum of one prior line of systemic therapy for unresectable advanced or metastatic ESCC.

You may not qualify if…

• Has prior treatment with B7-H3 targeted agent, including I-DXd.
• Has had prior discontinuation of an antibody drug conjugate (ADC) that consists of an exatecan derivative (e.g., trastuzumab deruxtecan) due to treatment-related toxicities.
• Has multiple primary malignancies within 3 years, except adequately resected non-melanoma skin cancer, curatively treated in situ disease, superficial GI tract tumors and non-muscle invasive bladder cancer curatively resected by endoscopic surgery.
• Uncontrolled significant cardiovascular disease
• Clinically severe pulmonary compromise resulting from intercurrent pulmonary illnesses including, but not limited to, any underlying pulmonary disorder, or any autoimmune, connective tissue or inflammatory disorders with potential pulmonary involvement, prior pneumonectomy, or requirement for supplemental oxygen
• Has an uncontrolled infection requiring systemic therapy.
• Has substance abuse or any other medical conditions that would increase the safety risk to the subject or interfere with participation of the subject or evaluation of the clinical study in the opinion of the Investigator.

Where it is running

• National Cancer Center Hospital East — Chiba, Japan (enrolling)
• Hokkaido University Hospital — Hokkaido, Japan (enrolling)
• Kobe City Medical Center General Hospital — Hyōgo, Japan (enrolling)
• Kagawa University Hospital — Kagawa, Japan (enrolling)
• The University of Osaka Hospital — Osaka, Japan (enrolling)
• Kindai University Hospital — Ōsaka-sayama, Japan (enrolling)
• Saitama Cancer Center — Saitama, Japan (enrolling)
• Shizuoka Cancer Center — Shizuoka, Japan (enrolling)
• National Cancer Center Hospital — Tokyo, Japan (enrolling)
• Cancer Institute Hospital of JFCR — Tokyo, Japan (enrolling)
• Showa Medical University Hospital — Tokyo, Japan (enrolling)
• Keio University Hospital — Tokyo, Japan (enrolling)
• Sarah Cannon Research Institute at HealthONE — Denver, Colorado, United States (enrolling)
• John Theurer Cancer Center at Hackensack University Medical Center — Hackensack, New Jersey, United States (enrolling)
• Florida Cancer Specialists — Sarasota, Florida, United States (enrolling)
• Aichi Cancer Center Hospital — Aichi, Japan (enrolling)
• MDACC (MD Anderson Cancer Center) — Houston, Texas, United States
• Florida Cancer Specialists — Orlando, Florida, United States
• Dana Farber Cancer Institute — Boston, Massachusetts, United States
• Henry Ford Hospital — Detroit, Michigan, United States
• Washington University — St Louis, Missouri, United States
• Columbia University Medical Center — New York, New York, United States
• Memorial Sloan-Kettering Cancer Center — New York, New York, United States
• The Ohio State University — Columbus, Ohio, United States
• Sidney Kimmel Cancer Center - Thomas Jefferson — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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