A Study of Varlilumab (Anti-CD27) and Ipilimumab and CDX-1401 in Patients With Unresectable Stage III or IV Melanoma

Part of paid clinical trials in San Francisco, California.

Sponsor
Celldex Therapeutics
Study ID
NCT02413827
Phase
PHASE1/PHASE2
Status
Terminated

Conditions

  • Unresectable Stage III or Stage IV Melanoma

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Combination of varlilumab and ipilimumab — DRUG
    Eligible patients will receive assigned treatments once every 3 weeks for a total of 4 treatments. Phase l dose: The planned dose of varlilumab will be dependent on the cohort assigned at enrollment. Varlilumab doses are 0.3 mg/kg or 3 mg/kg. Ipilimumab dose is 3 mg/kg.
  • Cohort A: varlilumab & ipilimumab; Cohort B: varlilumab, ipilimumab, CDX-1401 & poly-ICLC — DRUG
    Eligible patients will receive assigned treatments once every 3 weeks for a total of 4 treatments. Phase ll dose: The planned dose of varlilumab will be established from Phase I. Ipilimumab dose is 3 mg/kg. Patients assigned to receive CDX-1401 will receive a dose of 1 mg along with 2 mg poly-ICLC.

Study Details

This is a study to determine the clinical benefit (how well the drug works), safety and tolerability of combining a) varlilumab and ipilimumab and b) varlilumab, ipilimumab, CDX-1401 and poly-ICLC. The study will enroll patients with unresectable Stage III or Stage IV melanoma.

Key Dates

Start date
Apr 30, 2015
Status verified
Apr 2017
Primary completion
Nov 2, 2016
Completion
Nov 9, 2016

Study Design

Enrollment
9 participants (actual)
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Phase l: varlilumab and ipilimumab
  • Experimental: Phase ll: varlilumab & ipilimumab, +/- CDX-1401 & poly-ICLC.

Primary Outcome Measure

Phase l: Safety and tolerability of varlilumab in combination with ipilimumab as measured by incidences of drug related adverse events (AEs), serious drug related AEs, dose-limiting toxicities and laboratory test abnormalities. [ Time Frame: Safety follow-up is 70 days from last study drug dose. ]

Locations (8)

FacilityCityStateZIPSite coordinators
California Pacific Medical Center Research InstituteSan FranciscoCalifornia94115-
Sutter Pacific Medical FoundationSanta RosaCalifornia95403-
University of ColoradoAuroraColorado80045-
Georgetown University School of MedicineWashington D.C.District of Columbia20007-
University of ChicagoChicagoIllinois60637-
Washington University School of MedicineSt LouisMissouri63110-
University of Pittsburgh Medical CenterPittsburghPennsylvania15232-
Tennessee Oncology Sarah Cannon Research InstituteNashvilleTennessee37203-

Find similar trials in San Francisco, CA