LXE408 + sodium stibogluconate + Paromomycin

Phase 2Completed
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52
Hype Score

Development Stage

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

Primary Visceral Leishmaniasis

Conditions

Primary Visceral Leishmaniasis

Trial Timeline

Mar 29, 2024 → Nov 13, 2025

About LXE408 + sodium stibogluconate + Paromomycin

LXE408 + sodium stibogluconate + Paromomycin is a phase 2 stage product being developed by Novartis for Primary Visceral Leishmaniasis. The current trial status is completed. This product is registered under clinical trial identifier NCT05957978. Target conditions include Primary Visceral Leishmaniasis.

Hype Score Breakdown

Clinical
17
Activity
12
Company
10
Novelty
5
Community
5

Clinical Trials (1)

NCT IDPhaseStatus
NCT05957978Phase 2Completed

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