Efficacy Study of Pre-operative IPH2201 in Patients With Squamous Cell Carcinoma of the Oral Cavity

PHASE1/PHASE2TerminatedINTERVENTIONAL
Enrollment

3

Participants

Timeline

Start Date

December 31, 2014

Primary Completion Date

December 31, 2016

Study Completion Date

December 31, 2016

Conditions
Squamous Cell Carcinoma of the Oral Cavity
Interventions
DRUG

IPH2201

The first 6 patients will receive IPH2201, IV, at a dose of 4 mg/kg q2w x 4. Subsequent patients will be treated at a dose of 10 mg/kg q2w x 4.

PROCEDURE

Standard Surgery

After the end of treatment with IPH2201, according to standard recommendations in the relevant country .

RADIATION

Postsurgical Adjuvant Therapy

After the standard surgery, according to standard recommendations in the relevant country

Trial Locations (3)

13353

Charité University Medicine Berlin, Berlin

28047

Hospital Universitario La Paz, Madrid

08907

Instituto Catalan de Oncologia - L'Hospitalet, L'Hospitalet de Llobregat Barcelona

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Innate Pharma

INDUSTRY