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

2018년 5월 14일 업데이트: Cascadian Therapeutics Inc.

Phase 1/2 Study of PI-3K Inhibition With PX-866 Combined With Vemurafenib (BRAF Inhibitor) in Patients With BRAF-mutant Cancer Including Advanced Melanoma

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.

연구 개요

상세 설명

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.

연구 유형

중재적

등록 (실제)

24

단계

  • 2 단계
  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Florida
      • Tampa, Florida, 미국, 33612
        • H. Lee Moffitt Cancer Center
    • New York
      • New York, New York, 미국, 10016
        • New York University
    • Pennsylvania
      • Philadelphia, Pennsylvania, 미국, 19104
        • University of Pennsylvania
      • Pittsburgh, Pennsylvania, 미국, 15232
        • University of Pittsburgh Cancer Institute
    • Tennessee
      • Nashville, Tennessee, 미국, 37232
        • Vanderbilt-Ingram Cancer Center

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Phase 1 Dose Escalation of PX-866 + vemurafenib
PX-866 given with vemurafenib

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.

다른 이름들:
  • PI-3K inhibitor
vemurafenib is a B-Raf enzyme inhibitor
다른 이름들:
  • 젤보라프
실험적: Phase 2 Combination PX-866 + vemurafenib
PX-866 given with vemurafenib

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.

다른 이름들:
  • PI-3K inhibitor
vemurafenib is a B-Raf enzyme inhibitor
다른 이름들:
  • 젤보라프
활성 비교기: Phase 2 Single-agent vemurafenib
vemurafenib given as a single agent
vemurafenib is a B-Raf enzyme inhibitor
다른 이름들:
  • 젤보라프

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
Incidence and severity of adverse events (phase 1)
기간: 28 days
28 days
Progression-free survival (PFS) (phase 2)
기간: 56 days
56 days

2차 결과 측정

결과 측정
기간
Plasma concentrations of PX-866 and metabolites (phase 1)
기간: 44 days
44 days
Objective Response Rate (ORR)(phase 2)
기간: 56 days
56 days
Disease Control Rate (DCR)(phase 2)
기간: 56 Days
56 Days
Plasma concentrations of vemurafenib (phase 1)
기간: 44 days
44 days

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2012년 8월 1일

기본 완료 (실제)

2014년 12월 1일

연구 완료 (실제)

2015년 3월 1일

연구 등록 날짜

최초 제출

2012년 6월 6일

QC 기준을 충족하는 최초 제출

2012년 6월 7일

처음 게시됨 (추정)

2012년 6월 11일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2018년 5월 16일

QC 기준을 충족하는 마지막 업데이트 제출

2018년 5월 14일

마지막으로 확인됨

2015년 7월 1일

추가 정보

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

PX-866에 대한 임상 시험

구독하다