Oral Lenacapavir (LEN) + F/TDF + Sub-cutaneous (SC) Lenacapavir (LEN) + Placebo SC LEN + PTM F/TDF + PTM Oral LEN + F/TAF (for US participants only)

Phase 3Active
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76
Hype Score

Development Stage

โœ“
Pre-clinical
โœ“
Phase 1
โœ“
Phase 2
4
Phase 3
5
Approved
Indication / Disease

Pre-Exposure Prophylaxis of HIV Infection

Conditions

Pre-Exposure Prophylaxis of HIV Infection

Trial Timeline

Jun 28, 2021 โ†’ Aug 1, 2028

About Oral Lenacapavir (LEN) + F/TDF + Sub-cutaneous (SC) Lenacapavir (LEN) + Placebo SC LEN + PTM F/TDF + PTM Oral LEN + F/TAF (for US participants only)

Oral Lenacapavir (LEN) + F/TDF + Sub-cutaneous (SC) Lenacapavir (LEN) + Placebo SC LEN + PTM F/TDF + PTM Oral LEN + F/TAF (for US participants only) is a phase 3 stage product being developed by Gilead Sciences for Pre-Exposure Prophylaxis of HIV Infection. The current trial status is active. This product is registered under clinical trial identifier NCT04925752. Target conditions include Pre-Exposure Prophylaxis of HIV Infection.

Hype Score Breakdown

Clinical
27
Activity
18
Company
9
Novelty
9
Community
10

Clinical Trials (1)

NCT IDPhaseStatus
NCT04925752Phase 3Active