Study of PX-866 and Vemurafenib in Patients With Advanced Melanoma

NCT ID: NCT01616199

Last Updated: 2018-05-16

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-08-31
• Study Completion Date: 2015-03-31

Brief Summary

The purpose of the phase 1 portion of the study is to determine the maximally tolerated dose (MTD) or recommended dose (RD) and the safety/tolerability of PX-866 in combination vemurafenib in patients with any advanced BRAF-mutant cancer.

The purpose of the phase 2 portion of the study is to compare progression free survival (PFS), antitumor activity (response rate), disease control rate (DCR), and the safety and tolerability of PX-866 in combination with vemurafenib vs. vemurafenib alone in patients with advanced BRAF-mutant melanoma at the doses recommended from Phase 1.

Detailed Description

This is a Phase 1 / 2 open-label study of PX-866 given in combination with vemurafenib to patients with BRAF-mutant cancer, including advanced melanoma.

Phase 1 will use a 3+3 dose escalation design to evaluate up to three dose levels of PX-866 in combination with up to two dose levels of vemurafenib in order to identify the maximal tolerated dose/recommended dose (MTD/RD) of both PX-866 and vemurafenib to be used in Phase 2. Vemurafenib will be administered orally twice per day on days 1-28 of all cycles except cycle 1, where vemurafenib will be administered on days 9-28 to allow for PK assessments). PX-866 will be administered once per day on days 1-28 of each cycle.

Phase 2 will evaluate the antitumor activity and safety of PX-866 given to patients randomized 2:1 to receive combination with vemurafenib at the doses recommended from Phase 1 compared with vemurafenib alone administered at the approved dose orally BID. All treatments will be administered on a 28-day cycle.

Patients randomized to receive single-agent vemurafenib may cross-over to receive the combination treatment at the time of progression. Patients will be evaluated for progression approximately every 8 weeks for the initial 24 weeks and every 12 weeks thereafter. All patients with stable disease (SD) or better, will receive repeat cycles until disease progression (PD), unacceptable toxicity, or withdrawal of consent.

Conditions

Advanced BRAF-mutant Cancers

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Phase 1 Dose Escalation of PX-866 + vemurafenib

PX-866 given with vemurafenib

Group Type: EXPERIMENTAL

PX-866

Intervention Type: DRUG

Phase 1 dose escalation: PX-866 in combination administered orally every day in 28-day cycles until progression or unacceptable toxicity.

Phase 2 combination: PX-866 and vemurafenib administered every day in 28 day cycles until progression or unacceptable toxicity.

Phase 2 single-agent: vemurafenib administered orally at labeled dose every day in 28 day cycles until progression or unacceptable toxicity.

vemurafenib

Intervention Type: DRUG

vemurafenib is a B-Raf enzyme inhibitor

Phase 2 Combination PX-866 + vemurafenib

PX-866 given with vemurafenib

Group Type: EXPERIMENTAL

PX-866

Intervention Type: DRUG

Phase 1 dose escalation: PX-866 in combination administered orally every day in 28-day cycles until progression or unacceptable toxicity.

Phase 2 combination: PX-866 and vemurafenib administered every day in 28 day cycles until progression or unacceptable toxicity.

Phase 2 single-agent: vemurafenib administered orally at labeled dose every day in 28 day cycles until progression or unacceptable toxicity.

vemurafenib

Intervention Type: DRUG

vemurafenib is a B-Raf enzyme inhibitor

Phase 2 Single-agent vemurafenib

vemurafenib given as a single agent

Group Type: ACTIVE_COMPARATOR

vemurafenib

Intervention Type: DRUG

vemurafenib is a B-Raf enzyme inhibitor

Interventions

PX-866

Phase 1 dose escalation: PX-866 in combination administered orally every day in 28-day cycles until progression or unacceptable toxicity.

Phase 2 combination: PX-866 and vemurafenib administered every day in 28 day cycles until progression or unacceptable toxicity.

Phase 2 single-agent: vemurafenib administered orally at labeled dose every day in 28 day cycles until progression or unacceptable toxicity.

Intervention Type: DRUG

vemurafenib

vemurafenib is a B-Raf enzyme inhibitor

Intervention Type: DRUG

Other Intervention Names

PI-3K inhibitor; Zelboraf

Eligibility Criteria

Inclusion Criteria

• ≥ 18 years at time of consent
• If a sexually active male or a sexually active female of child-bearing potential, agrees to use a highly effective form of contraception (including birth control pills, barrier device, or intrauterine device)from the time of consent 90 days following the last dose of study drug
• If female of child-bearing potential, negative pregnancy test
• For Phase 1: must have histologically or cytologically-confirmed advanced cancer that is BRAF mutation-positive (V600E or V600K) for which there is no remaining standard therapy with curative potential. Patients must have disease sites amenable to biopsy. For Phase 2: must have histologically or cytologically-confirmed BRAF mutation-positive (V600E or V600K) advanced (defined as unresectable Stage IIIC or IV) melanoma that has not been treated with a selective BRAF inhibitor
• For Phase 1: must have measurable or non-measurable disease. For Phase 2: must have measurable disease per RECIST 1.1
• For Phase 1: no restriction on number of prior therapy regimens. For Phase 2: the following restrictions on prior therapy apply: 1) must not have been treated with a selective BRAF inhibitor and must not have had more than 2 prior treatment regimens for advanced metastatic disease; 2) must have completed prior cytotoxic chemotherapy a minimum of 4 weeks prior to starting PX-866 and/or vemurafenib (except for BCNU and/or mitomycin C, which must have been completed a minimum of 6 weeks prior to starting therapy). Prior biologic therapy and localized radiation therapy must have been completed a minimum of 2 weeks prior to starting therapy.
• All toxicities related to prior cancer therapies other than alopecia must have resolved to Grade 1 or less
• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
• In the opinion of the clinical investigator, life expectancy > 3 months
• Adequate hematologic function
• Adequate hepatic function
• Serum creatinine < 2.0 mg/dL
• Adequate cardiac function
• Corrected QTc must be <480 milliseconds

Exclusion Criteria

• May not be receiving any other investigational agents
• Active central nervous system (CNS) metastases are excluded. Patients with a history of CNS metastasis, who have been treated prior to enrollment, must be stable for eight weeks after completion of treatment. These patients must have undergone appropriate imaging studies and currently be on a stable, lowest possible dose of steroids
• History of allergic reactions attributed to compounds of similar chemical or biologic composition to PX-866 or vemurafenib
• Uncontrolled intercurrent illness including, but not limited to: ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
• Uncorrectable electrolyte abnormalities or long QT syndrome
• Poorly controlled diabetes mellitus
• Pregnant, breastfeeding, or planning to become pregnant
• Known to be human immunodeficiency virus (HIV)-positive
• Inability to swallow pills
• Previous treatment with a phosphatidylinositol-3-kinase (PI-3K) inhibitor
• Any other significant medical or psychiatric condition that in the opinion of the investigator renders the patient inadequate for participation

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Cascadian Therapeutics Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

H. Lee Moffitt Cancer Center

Tampa, Florida, United States

New York University

New York, New York, United States

University of Pennsylvania

Philadelphia, Pennsylvania, United States

University of Pittsburgh Cancer Institute

Pittsburgh, Pennsylvania, United States

Vanderbilt-Ingram Cancer Center

Nashville, Tennessee, United States

Countries

United States

Other Identifiers

PX-866-007

Identifier Type: -

Identifier Source: org_study_id