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temsirolimus

Generic: TEMSIROLIMUS·Brand: TEMSIROLIMUS, TORISEL, Torisel

temsirolimus: 6 clinical trials tracked.

temsirolimus evidence translation

What we can confirm

6 tracked trials

No verified listed company relationship

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 temsirolimus, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence8 indications · 1 study sponsors
Clinical Trial Registry Records (6)

Pilot Trial of an Implantable Microdevice for In Vivo Drug Sensitivity Testing in Patients With Sarcomas

NCT04199026Registry updated 2026-02-19·N/A
Recruiting

Primary endpoint: Determination of the safety and technical feasibility of microdevice insertion/removal, as assessed by adverse events by CTCAE 5.0.

Interventionalopen20 targetStarted 2025-02Completion 2028-121 site · United StatesM.D. Anderson Cancer Center

Canadian Profiling and Targeted Agent Utilization Trial (CAPTUR): A Phase II Basket Trial

NCT03297606Registry updated 2026-03-27·Phase 2
Recruiting

Primary endpoint: Objective response rate defined as the number of patients with complete response or partial response

Interventionalopen720 targetStarted 2018-03Completion 2027-0110 sites · CanadaCanadian Cancer Trials Group

Therapeutic Trial for Patients With Ewing Sarcoma Family of Tumor and Desmoplastic Small Round Cell Tumors

NCT01946529Registry updated 2026-08-21·Phase 2
Completed

Primary endpoint: Response to Window Therapy (2 Courses) for Group B (High-risk) - ESFT Participants

Interventionalopen24 enrolledStarted 2013-12Completion 2026-041 site · United StatesSt. Jude Children's Research Hospital

A Phase I Trial of Bevacizumab, Temsirolimus Alone and in Combination With Valproic Acid, or Cetuximab in Patients With Advanced Malignancy and Other Indications

NCT01552434Registry updated 2026-04-24·Phase 1
Active, not recruiting

Primary endpoint: Maximum tolerated dose (MTD) of bevacizumab, defined as the dose level below the dose at which 2 of 6 patients experience drug-related dose limiting toxicity (DLT)

Interventionalopen155 targetStarted 2012-10Completion 2026-101 site · United StatesM.D. Anderson Cancer Center

A Phase II Study of Sunitinib or Temsirolimus in Patients With Advanced Rare Tumours

NCT01396408Registry updated 2026-08-11·Phase 2
Active, not recruiting

Primary endpoint: Objective Response

Interventionalopen137 enrolledStarted 2012-02Completion 2026-1217 sites · CanadaCanadian Cancer Trials Group

A Phase I, Open-Label, Multi-center Study to Assess the Safety, Tolerability and Pharmacokinetics of AZD6244 (ARRY-142886) When Given in Combination With Standard Doses of Selected Chemotherapies to Patients With Advanced Solid Tumors

NCT00600496Registry updated 2026-05-27·Phase 1·AZN
Completed

Primary endpoint: Safety and tolerability of twice daily oral doses of AZD6244 when administered in combination with standard doses of selected chemotherapies.

Interventionalopen140 enrolledStarted 2007-12Completion 2025-124 sites · United StatesAstraZeneca