Melanoma Clinical Trial

A Phase 1b/2a Study Evaluating AMG 232 in Metastatic Melanoma

Summary

Phase 1b/2a, open-label, sequential dose escalation and expansion study of AMG 232 in combination with trametinib and dabrafenib in subjects with metastatic melanoma followed by a direct comparison of AMG 232 combined with trametinib and dabrafenib versus trametinib combined with dabrafenib alone.

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Full Description

The study will be conducted in 3 parts: Part 1 - Dose Escalation, Part 2 - Dose Expansion and Part 3, a randomized Phase 2a.

In both part 1 and 2, subjects will be enrolled open-label into 1 of 2 arms. For both Arm 1 and Arm 2, the part 1 dose escalation is aimed at determining an AMG 232 maximum tolerated dose (MTD) with a fixed dose of the combination drug(s) and evaluating safety, tolerability, pharmacokinetics and pharmacodynamics of each combination. Part 2 dose expansion will enroll subjects to receive therapy with a dose and schedule of AMG 232 selected from the corresponding part 1 dose escalation. In part 2 subjects will be enrolled to confirm safety and tolerability and to assess clinical activity prior to proceeding to Part 3, Phase 2a. In Phase 2a, Subjects will be randomized open-label in a 1:1 ratio to receive AMG 232 in combination with trametinib plus dabrafenib versus trametinib plus dabrafenib alone.

Only Part 1 of the study was enrolled and the study did not proceed into Phase 2.

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Eligibility Criteria

Inclusion Criteria: Subjects must have histologically or cytologically confirmed metastatic cutaneous or mucosal melanoma, Able to swallow and retain orally administered medication, Adequate hematological, renal, hepatic, and coagulation laboratory assessments Exclusion Criteria: Clinically significant bleeding within 4 weeks of screening, Current use of warfarin, factor Xa inhibitors, and direct thrombin inhibitors, Infection requiring anti-infective treatments within 1 week of study enrollment, Anti-tumor therapy, Major surgery within 28 days

Study is for people with:

Melanoma

Phase:

Phase 1

Estimated Enrollment:

31

Study ID:

NCT02110355

Recruitment Status:

Completed

Sponsor:

Kartos Therapeutics, Inc.

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There are 7 Locations for this study

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Research Site
Los Angeles California, 90095, United States
Research Site
Aurora Colorado, 80045, United States
Research Site
Boston Massachusetts, 02114, United States
Research Site
Chapel Hill North Carolina, 27599, United States
Research Site
Nashville Tennessee, 37232, United States
Research Site
North Sydney New South Wales, 2060, Australia
Research Site
Melbourne Victoria, 3000, Australia

How clear is this clinincal trial information?

Study is for people with:

Melanoma

Phase:

Phase 1

Estimated Enrollment:

31

Study ID:

NCT02110355

Recruitment Status:

Completed

Sponsor:


Kartos Therapeutics, Inc.

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