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OncoMatch/Clinical Trials/NCT07890714

A Study of Dato-DXd in Participants With Solid Tumors [TROPION-PanTumor04 (TP04)]

Official title: A Phase 1/2, Multicenter, Master Protocol Trial to Evaluate the Efficacy and Safety of Datopotamab Deruxtecan (Dato-DXd) in Participants With Solid Tumors (TROPION-PanTumor04)

Is NCT07890714 recruiting? Yes, currently enrolling (Oct 2026). This Phase 1/2 trial studies multiple treatments including Dato-DXd and Enfortumab Vedotin (EV) for urothelial cancer.

Phase 1/2RecruitingDaiichi SankyoNCT07890714Data as of Oct 2026Location: Taiwan

Treatment: Dato-DXd · Enfortumab Vedotin (EV) · Pembrolizumab · Olomorasib — This clinical trial is designed to assess the safety, tolerability, and antitumor activity of Datopotamab Deruxtecan (Dato-DXd) combined with other anticancer agents or as monotherapy in participants with solid tumors.

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Extracted eligibility criteria

Treatments studied

Immunotherapy

Pembrolizumab

Targeted therapy

Enfortumab Vedotin (EV)

Other

Dato-DXdOlomorasib

Cancer type

Urothelial Carcinoma

Non-Small Cell Lung Carcinoma

Performance status

ECOG 0–1(Restricted strenuous activity)

Lab requirements

Blood counts

adequate organ and bone marrow function as assessed by local laboratory within 7 days prior to C1D1 (randomization for randomized cohort) as defined in the protocol

Kidney function

adequate organ and bone marrow function as assessed by local laboratory within 7 days prior to C1D1 (randomization for randomized cohort) as defined in the protocol

Liver function

adequate organ and bone marrow function as assessed by local laboratory within 7 days prior to C1D1 (randomization for randomized cohort) as defined in the protocol

Cardiac function

left ventricular ejection fraction (LVEF) ≥50% by ECHO or MUGA within 28 days before C1D1

Has adequate organ and bone marrow function as assessed by local laboratory within 7 days prior to C1D1 (randomization for randomized cohort) as defined in the protocol. Has a left ventricular ejection fraction (LVEF) ≥50 percent (%) by either an echocardiogram (ECHO) or multigated acquisition scan (MUGA) scan within 28 days before C1D1 (randomization for randomized cohort).

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT07890714 currently recruiting?

Yes, this trial is currently recruiting patients.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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