A Prospective, Open Phase I Study to Investigate the Tolerability and Efficacy of ALECSAT to Pancreas Cancer Patients

PHASE1CompletedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

October 31, 2013

Primary Completion Date

January 31, 2015

Study Completion Date

September 30, 2015

Conditions
Pancreatic Cancer
Interventions
BIOLOGICAL

Alecsat

The ALECSAT CBMP will be administered as single dose at week 4, 7 and week 10 which is considered an appropriate time for ALECSAT CBMP to strengthen the immune system and thus have the ability to kill tumour cells. It is the aim that the patients will receive three doses during the study period however, if the patient wish and it is recommended by the investigator, patients may receive more than three doses, continuing until progression or as judged by the Investigator. Continued treatment after the 24 week study period is only possible under the condition that no safety issues have been discovered. The interval between injections for continued treatment will be decided based on e.g. tumour response and clinical examinations.

Trial Locations (1)

DK-2400

Kirurgisk afdeling K, Bispebjerg Hospital, Copenhagen

All Listed Sponsors
lead

CytoVac A/S

INDUSTRY

NCT01984658 - A Prospective, Open Phase I Study to Investigate the Tolerability and Efficacy of ALECSAT to Pancreas Cancer Patients | Biotech Hunter | Biotech Hunter