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Clinical Trials/NL-OMON48820
NL-OMON48820CompletedPhase 2

An Open Label Phase II Study of Tipifarnib in Advanced Non-Hematological Malignancies with HRAS Mutations. - Tipifarnib Phase II Study-KO-TIP-001

Kura Oncology, Inc0 sites6 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 2
Status
Completed
Enrollment
6

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 to 64 (—)

Inclusion Criteria

  • - Subject is at least 18 years of age.
  • - Subject has a histologically or cytologically confirmed diagnosis of non-hematological malignancy for which there is no curative therapy available
  • - Subject has a tumor that carries a missense HRAS mutation according to a methodology approved by the Sponsor.
  • - Subject has measurable disease according to RECIST v1.1 and has relapsed (progressive disease) or is refractory to prior therapy

Exclusion Criteria

  • - Ongoing treatment with an anticancer agent not contemplated in this protocol.
  • - Prior treatment (at least 1 full treatment cycle) with an FTase inhibitor.
  • - Concomitant disease or condition that could interfere with the conduct of the study, or that would, in the opinion of the Investigator, pose an unacceptable risk to the subject in this study

Investigators

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