Study identification

EU PAS number

EUPAS42609

Study ID

49488

Official title and acronym

C2C: COMBINE-2 for Cabotegravir+Rilpivirine LA Regimen - A Prospective Cohort Study to Monitor Effectiveness, Adherence and Resistance (215160)

DARWIN EU® study

No

Study countries

Belgium
France
Germany
Italy
Netherlands
Spain
Sweden
Switzerland
United Kingdom

Study description

This prospective cohort study will gather real world evidence in routine clinical practice to evaluate the CAB+RPV LA regimen. The study will assess effectiveness, discontinuation, and resistance over 24-months of follow-up period in patients living with HIV.

Study status

Ongoing
Research institutions and networks

Institutions

ViiV Healthcare
First published:
01/02/2024
Institution

Contact details

GSK Clinical Disclosure Advisor

Primary lead investigator
Study timelines

Date when funding contract was signed

Planned:
Actual:

Study start date

Planned:
Actual:

Date of final study report

Planned:
Sources of funding
Pharmaceutical company and other private sector 

More details on funding

ViiV Healthcare & Janssen
Regulatory

Was the study required by a regulatory body?

Yes

Is the study required by a Risk Management Plan (RMP)?

EU RMP category 3 (required)