Ozmosi | STSA-1005 Drug Profile
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STSA-1005

Alternative Names: stsa-1005, stsa 1005, stsa1005
Clinical Status: Inactive
Latest Update: 2024-05-22
Latest Update Note: Clinical Trial Update

Product Description

STSA-1005 is being developed by Staidson (Beijing) Biopharmaceuticals for the treatment of severe COVID-19 indications. (Sourced from: https://www.staidsonbio.com/stsa-1005-injection-gains-approval-from-the-u-s-fda-to-conduct-clinical-trials/)

Mechanisms of Action: GM-CSF Blocker

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Injection

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Staidson Biopharma
Company Location: Asia Pacific
Company CEO:
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 1: Healthy Volunteers

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT05559125

STSA-1002/1005-01

P1

Terminated

Healthy Volunteers

2024-03-26

12%

2024-05-23

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

NCT05085197

STSA-1005-01

P1

Completed

Healthy Volunteers

2022-04-05

12%

2022-04-19

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

Recent News Events

Date

Type

Title