Dose-escalation Study of LTX-315 in Patients With a Transdermally Accessible Tumour

PHASE1CompletedINTERVENTIONAL
Enrollment

14

Participants

Timeline

Start Date

January 31, 2010

Primary Completion Date

January 31, 2013

Study Completion Date

January 31, 2013

Conditions
Cancer With Transdermal Accessible Tumour
Interventions
DRUG

LTX-315 (Oncopore™)

5 mg/ml-70 mg/ml. Dosing will be done as transdermal injection of a calculated volume at day 1 and 8. Additionally weekly injections up to a maximum of 4 injections.

Trial Locations (2)

0310

Oslo University Hospital, Radiumhospitalet, Oslo

171 76

Karolinska University Hospital, Solna, Stockholm

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Oslo University Hospital

OTHER

collaborator

Karolinska University Hospital

OTHER

lead

Lytix Biopharma AS

INDUSTRY

NCT01058616 - Dose-escalation Study of LTX-315 in Patients With a Transdermally Accessible Tumour | Biotech Hunter | Biotech Hunter