OMO1.01.02
Research type
Research Study
Full title
A modular, multi-arm, multi-part, first time in patient study to evaluate the safety and tolerability of OMO-1, alone and in combination with anti-cancer treatments, in patients with locally advanced, unresectable or metastatic solid malignancies
IRAS ID
225742
Contact name
Sarah Patricia Blagden
Contact email
Sponsor organisation
OCTIMET Oncology NV
Eudract number
2017-000878-11
Duration of Study in the UK
2 years, 2 months, 28 days
Research summary
A clinical study to investigate study drug OMO-1 with patients diagnosed with advanced inoperable or metastatic cancer.
REC name
South Central - Oxford C Research Ethics Committee
REC reference
17/SC/0229
Date of REC Opinion
8 Jun 2017
REC opinion
Further Information Favourable Opinion