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dactinomycin

Generic: DACTINOMYCIN·Brand: COSMEGEN, Cosmegen, DACTINOMYCIN

dactinomycin: 7 clinical trials tracked.

dactinomycin evidence translation

What we can confirm

7 tracked trials

No verified listed developer

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about dactinomycin, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence1 indications · 2 study sponsors
Clinical Trials (7)

A Randomized Phase 3 Study to Compare VAC (Higher Cyclophosphamide Dose and Intensity) Versus VAC/VI (Lower Cyclophosphamide Dose and Intensity) Plus Maintenance Therapy in Patients With Newly Diagnosed Intermediate-Risk Rhabdomyosarcoma

NCT07466316·Phase 3
Recruiting

Primary endpoint: Event free survival (EFS)

InterventionalRandomizedopen342 targetStarted 2026-07Completion 2031-0350 sites · United StatesChildren's Oncology Group

Prospective Treatment of Types I, II and III Pleuropulmonary Blastoma (PPB)

NCT06647953·Phase 3
Recruiting

Primary endpoint: Objective response

Interventionalopen110 targetStarted 2025-03Completion 2029-0350 sites · United StatesChildren's Oncology Group

A Randomized Phase 3 Trial of Vinorelbine, Dactinomycin, and Cyclophosphamide (VINO-AC) Plus Maintenance Chemotherapy With Vinorelbine and Oral Cyclophosphamide (VINO-CPO) vs Vincristine, Dactinomycin and Cyclophosphamide (VAC) Plus VINO-CPO Maintenance in Patients With High Risk Rhabdomyosarcoma (HR-RMS)

NCT04994132·Phase 3
Active, not recruiting

Primary endpoint: Event-free survival (EFS)

InterventionalRandomizedopen113 enrolledStarted 2021-09Completion 2027-0750 sites · United StatesChildren's Oncology Group

Risk-Adapted Focal Proton Beam Radiation and/or Surgery in Patients With Low, Intermediate and High Risk Rhabdomyosarcoma Receiving Standard or Intensified Chemotherapy

NCT01871766·Phase 2·GHRS
Active, not recruiting

Primary endpoint: Event-free survival (intermediate risk arm)

Interventionalopen115 targetStarted 2013-12Completion 2030-064 sites · United StatesSt. Jude Children's Research Hospital

Treatment for Patients With Bilateral, Multicentric, or Bilaterally-Predisposed Unilateral Wilms Tumor

NCT00945009·Phase 3·CGON
Completed

Primary endpoint: Event-Free Survival (EFS)

Interventionalopen249 enrolledStarted 2009-08Completion 2026-0350 sites · United StatesChildren's Oncology Group

Treatment of Newly Diagnosed Higher Risk Favorable Histology Wilms Tumors

NCT00379340·Phase 3
Completed

Primary endpoint: Event Free Survival Probability

Interventionalopen395 enrolledStarted 2007-04Completion 2026-0350 sites · United StatesChildren's Oncology Group

Treatment for Very Low and Standard Risk Favorable Histology Wilms Tumor

NCT00352534·Phase 3·CGON
Completed

Primary endpoint: Event Free Survival Probability

Interventionalopen808 enrolledStarted 2006-11Completion 2026-0350 sites · United StatesChildren's Oncology Group