Gyre Therapeutics, Inc., a pharmaceutical company, engages in the development and commercialization of small-molecule, anti-inflammatory, and anti-fibrotic drugs targeting organ fibrosis. The company offers ETUARY (Pirfenidone), an anti-fibrotic drug approved for the treatment of idiopathic pulmonary fibrosis; and under Phase 3 trials for the treatment of pneumoconiosis. It is also involved in the development of F351 (Hydronidone), a structural derivative of ETUARY, under Phase 3 trials for the treatment of chronic hepatitis B (CHB)-associated liver fibrosis; and completed Phase 1 trials for the treatment of liver fibrosis associated with metabolic dysfunction-associated steatohepatitis. In addition, the company develops F573 is in Phase 2 clinical trials for the treatment of acute/acute-on-chronic liver failure. Further, its preclinical products include F230 for the treatment of pulmonary arterial hypertension; and F528 to treat chronic obstructive pulmonary disease. Gyre Therapeutics, Inc. was founded in 2002 and is headquartered in San Diego, California. Gyre Therapeutics, Inc. operates as a subsidiary of GNI USA, Inc. Show more

12770 High Bluff Drive, San Diego, CA, 92130, United States

Biotechnology
Healthcare

Market Cap

691.7M

52 Wk Range

$6.11 - $11.78

Previous Close

$7.18

Open

$7.01

Volume

35,927

Day Range

$7.01 - $7.28

Enterprise Value

560.3M

Cash

52.43M

Avg Qtr Burn

-5.625M

Insider Ownership

86.70%

Institutional Own.

3.69%

Qtr Updated

12/31/25


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Drug & IndicationStage & EventCatalyst Date

Approved

Quarterly sales

Avatrombopag Details
Thrombocytopenia , Chronic liver disease

Approved

Quarterly sales

F351 (Hydronidone) Details
Chronic hepatitis B, Liver fibrosis

NDA

Submission

Phase 3

Data readout

Pirfenidone (Antifibrotic Agent) Details
Radiation-Induced Lung Injury And Immune-Related Pneumonitis

Phase 2/3

Initiation

F573 Details
Acute-on-Chronic liver failure

Phase 2

Data readout

F230 Details
Pulmonary arterial hypertension

Phase 1

Data readout

F528 (Unknown Mechanism) Details
Undisclosed Indication

Phase 1

Initiation

F351 (Hydronidone) Details
Non-alcoholic steatohepatitis , Liver fibrosis

IND

Submission

F351 (Hydronidone) Details
Metabolic dysfunction-associated steatohepatitis (“MASH”)-related fibrosis

IND

Submission