Phase 1/2 Study of Mocetinostat and Durvalumab in Patients With Advanced Solid Tumors and NSCLC

PHASE1/PHASE2TerminatedINTERVENTIONAL
Enrollment

83

Participants

Timeline

Start Date

June 1, 2016

Primary Completion Date

December 14, 2019

Study Completion Date

December 20, 2019

Conditions
Advanced Cancer
Interventions
DRUG

Mocetinostat - 50 mg

Participants received mocetinostat three times weekly as an oral capsule.

DRUG

Mocetinostat - 70 mg

Participants received mocetinostat three times weekly as an oral capsule.

DRUG

Mocetinostat - 90 mg

Participants received mocetinostat three times weekly as an oral capsule.

DRUG

Mocetinostat - Recommended Phase 2 Dose (70 mg)

Participants received mocetinostat three times weekly as an oral capsule, at the dose recommended after Phase 1 (70 mg).

DRUG

Durvalumab - 1500 mg

Participants received durvalumab as an intravenous infusion every 4 weeks.

Trial Locations (15)

10461

Montefiore Medical Center, The Bronx

22031

Virginia Cancer Specialists, Fairfax

22601

Shenandoah Oncology - Winchester, Winchester

32503

Woodlands Medical Specialists - Pensacola, Pensacola

36608

Southern Cancer Center, PC, Mobile

37203

Sarah Cannon Research Institute, Nashville

55414

Unniversity of Minnesota Masonic Cancer Center, Minneapolis

60201

NorthShore University Health System, Evanston

60611

Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago

75093

Texas Oncology-Plano West, Plano

75230

Mary Crowley Cancer Research Centers, Dallas

76210

Texas Oncology - Denton South, Denton

90095

David Geffen School of Medicine at UCLA, Los Angeles

98109

Seattle Cancer Care Alliance, Seattle

07601

Hackensack University Medical Center, Hackensack

Sponsors
All Listed Sponsors
lead

Mirati Therapeutics Inc.

INDUSTRY

NCT02805660 - Phase 1/2 Study of Mocetinostat and Durvalumab in Patients With Advanced Solid Tumors and NSCLC | Biotech Hunter | Biotech Hunter