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

14 mai 2018 mis à jour par: 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.

Aperçu de l'étude

Statut

Résilié

Description détaillée

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.

Type d'étude

Interventionnel

Inscription (Réel)

24

Phase

  • Phase 2
  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

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

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans et plus (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

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

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 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.

Autres noms:
  • PI-3K inhibitor
vemurafenib is a B-Raf enzyme inhibitor
Autres noms:
  • Zelboraf
Expérimental: 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.

Autres noms:
  • PI-3K inhibitor
vemurafenib is a B-Raf enzyme inhibitor
Autres noms:
  • Zelboraf
Comparateur actif: Phase 2 Single-agent vemurafenib
vemurafenib given as a single agent
vemurafenib is a B-Raf enzyme inhibitor
Autres noms:
  • Zelboraf

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
Incidence and severity of adverse events (phase 1)
Délai: 28 days
28 days
Progression-free survival (PFS) (phase 2)
Délai: 56 days
56 days

Mesures de résultats secondaires

Mesure des résultats
Délai
Plasma concentrations of PX-866 and metabolites (phase 1)
Délai: 44 days
44 days
Objective Response Rate (ORR)(phase 2)
Délai: 56 days
56 days
Disease Control Rate (DCR)(phase 2)
Délai: 56 Days
56 Days
Plasma concentrations of vemurafenib (phase 1)
Délai: 44 days
44 days

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

1 août 2012

Achèvement primaire (Réel)

1 décembre 2014

Achèvement de l'étude (Réel)

1 mars 2015

Dates d'inscription aux études

Première soumission

6 juin 2012

Première soumission répondant aux critères de contrôle qualité

7 juin 2012

Première publication (Estimation)

11 juin 2012

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

16 mai 2018

Dernière mise à jour soumise répondant aux critères de contrôle qualité

14 mai 2018

Dernière vérification

1 juillet 2015

Plus d'information

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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