IMP321 Plus First-line Paclitaxel in Metastatic Breast Carcinoma

PHASE1CompletedINTERVENTIONAL
Enrollment

33

Participants

Timeline

Start Date

July 31, 2006

Primary Completion Date

November 30, 2009

Study Completion Date

January 31, 2010

Conditions
Metastatic Breast Cancer
Interventions
BIOLOGICAL

IMP321

"This study is an open label, non-randomized, fixed dose-escalation phase I study, performed in ambulatory setting with patients receiving as a first line chemotherapy for metastatic breast carcinoma the standard 6 cycles of paclitaxel (80 mg/m² at D1, D8 and D15 of every 4-week cycle).~Three IMP321 dose levels (250 µg, 1,250 µg and 6,250 µg) will be evaluated in three cohorts of 8 patients. At any given dose level the patients will be administered one dose every two weeks for a total of 24 weeks (12 s.c. injections in total), separated by 13-day intervals free of IMP321 administration.~The repeated single doses will be administered on D2 and D16 of the 4-week cycles, on the day which follows chemotherapy."

Trial Locations (3)

75908

Hôpital Européen Georges Pompidou, Paris

92210

Centre René Huguenin, Saint-Cloud

Unknown

Hôpital Tenon, Paris

All Listed Sponsors
collaborator

Umanis

INDUSTRY

lead

Immutep S.A.S.

INDUSTRY

NCT00349934 - IMP321 Plus First-line Paclitaxel in Metastatic Breast Carcinoma | Biotech Hunter | Biotech Hunter