A Study of DS-3939a in Participants With Solid Tumors

Starting soon · Phase 1/Phase 2

Conditions studied: Solid Tumor, Locally Advanced Non-Small Cell Lung Cancer, Metastatic Non-Small Cell Lung Cancer

In brief

The primary purpose of the study is to evaluate the safety, tolerability, and efficacy of DS-3939a in combination with other anticancer agents or as a monotherapy in participants with solid tumors.

Key facts

Study ID

NCT07739966

Run by

Daiichi Sankyo

People needed

400

Starts

2026-10-01

Expected to finish

2032-01-29

Last updated by the study team

2026-07-31

Who can join

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

You may qualify if…

• Sign and date the Main Trial informed consent form (ICF), prior to the start of any trial-specific procedures.
• Adults greater than or equal to (≥)18 years of age at the time the Main Trial ICF is signed (follow local regulatory requirements if the legal age of consent for trial participation is >18 years old).
• Histologically documented Stage IIIB, IIIC disease who is not candidate for surgical resection or definitive chemoradiation, or Stage IV NSQ NSCLC.
• Has a left ventricular ejection fraction (LVEF) ≥50 percent (%) by either an echocardiogram (ECHO) or multigated acquisition scan (MUGA) within 28 days of the first trial intervention.
• Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1 assessed no more than 14 days prior to initiation of trial interventions.
• Has adequate organ function.
• Participants must have measurable disease by investigator assessment according to RECIST v1.1.
• Additional Inclusion Criteria for Substudy 1:
• Participants must not have received prior systemic therapy for locally advanced unresectable or metastatic NSCLC.
• Additional Inclusion Criteria for Substudy 2:
• Participants with AGA (excluding EGFR mutation): Participants have been previously treated with targeted therapy for the AGA and platinum-based chemotherapy for the advanced disease setting.
• Participants without AGA: Participants have been previously treated with platinum-based chemotherapy and anti-programmed death-1 (anti-PD-1)/programmed death-ligand 1 (PD-L1) antibody
• Part 2 only: Participants must have received only 1 or 2 prior lines of anticancer therapy for the advanced disease setting.

You may not qualify if…

• Prior systemic anticancer therapy targeting MUC1 or TA-MUC1.
• Prior systemic anticancer therapy with topoisomerase 1 inhibitor or topoisomerase 1 inhibitor-based antibody-drug conjugate (ADCs) (e.g., datopotamab deruxtexan and Sacituzumab govitecan).
• Has spinal cord compression or clinically active central nervous system (CNS) metastases.
• Has multiple primary malignancies.
• Has any history of interstitial lung disease (ILD)/pneumonitis irrespective of steroid use, or current ILD, or suspected ILD, or ILD that cannot be ruled out by imaging at screening
• Has active or uncontrolled human immunodeficiency virus (HIV) infection.
• Has active or uncontrolled hepatitis B virus (HBV)/hepatitis C virus (HCV) infection.
• Any of the following within the past 6 months: cerebrovascular accident, transient ischemic attack, or other arterial thromboembolic event.
• Current participation in other therapeutic investigational procedures, except for participation in long term survival follow-up (LTSFU) without any investigational treatment.

Full record on ClinicalTrials.gov

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