MHRA paediatric investigation plan
REKAMBYS (RILPIVIRINE)
MHRA paediatric investigation plan MHRA-100865-PIP01-23-M01 (update) · Modification
Key facts
| PIP number | MHRA-100865-PIP01-23-M01 (update) |
|---|---|
| Product names | REKAMBYS |
| Active substances | RILPIVIRINE |
| Therapeutic areas | Infectious diseases |
| Conditions | Treatment of human immunodeficiency virus (HIV-1) infection |
| Decision | PM: decision on the application for modification of an agreed paediatric investigation plan. |
| Compliance check outcome | Partial |
| Published | Dec 19, 2023 |
| MHRA record | cms.mhra.gov.uk |
About MHRA paediatric investigation plans
A paediatric investigation plan sets out the studies a company must run in children to support authorisation of a medicine in the UK, or records a waiver or deferral.
Source: UK Medicines and Healthcare products Regulatory Agency (MHRA). Contains public sector information licensed under the Open Government Licence v3.0 · Source date: