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Clinical Trial Summary

Phase 1 and 2 trial to study the safety, pharmacokinetics, and efficacy of TAS0953/HM06 in patients with advanced solid tumors with RET gene abnormalities. Phase 1 aims to determine the Maximum Tolerated Dose (MTD) and identify the Recommended Phase 2 Dose (RP2D) to be used in phase 2.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04683250
Study type Interventional
Source Helsinn Healthcare SA
Contact Michael Karl
Phone +49 8709 943 761
Email Michael.Karl@iconplc.com
Status Recruiting
Phase Phase 1/Phase 2
Start date December 16, 2020
Completion date September 2025

See also
  Status Clinical Trial Phase
Completed NCT03037385 - Phase 1/2 Study of the Highly-selective RET Inhibitor, Pralsetinib (BLU-667), in Participants With Thyroid Cancer, Non-Small Cell Lung Cancer, and Other Advanced Solid Tumors Phase 1/Phase 2
Recruiting NCT05653869 - A Study of APS03118 in Advanced Solid Tumors Harboring RET Mutations or Fusions Phase 1