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Lancovutide

Alternative Names: lancovutide, moli-1901, moli 1901, moli1901, duramycin
Latest Update: 2024-05-07
Latest Update Note: PubMed Publication

Product Description

Mechanisms of Action: TMEM16A Activator

Novel Mechanism: Yes

Modality: Peptide/Protein

Route of Administration: Inhalant

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: Indonesia | Taiwan

Approved Indications: None

Known Adverse Events: None

Company: AOP Orphan AG
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Lancovutide

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 3: Cystic Fibrosis

Phase 1: Oncology Unspecified|Healthy Volunteers

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

PicTURE

P1

Completed

Healthy Volunteers|Oncology Unspecified

2021-12-14

2005-005594-29

P3

Terminated

Cystic Fibrosis

2021-04-23

2006-006693-24

P3

Completed

Cystic Fibrosis

2009-07-15

Moli1901-010B

P2

Completed

Cystic Fibrosis

2009-07-01

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