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TD-101

Alternative Names: td-101, td101, td 101
Latest Update: 2008-11-19
Latest Update Note: Clinical Trial Update

Product Description

a Small Interfering RNA (siRNA) Designed for Treatment of Pachyonychia Congenita (Sourced from: https://clinicaltrials.gov/ct2/show/NCT00716014)

Mechanisms of Action: Mutant K6a Binder

Novel Mechanism: Yes

Modality: N/A

Route of Administration: Injection

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Pachyonychia Congenita Project
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for TD-101

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 1: Pachyonychia Congenita

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success
NCT00716014

P1

Completed

Pachyonychia Congenita

2008-08-01

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