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Sunhawk Vision Mandated by Global Mega-Pharma Titans for Exclusive One-on-One Closed-Door Summits at BIO 2026 to Leverage Strategic Licensing and Equity Bids for SHJ002 Platform.

The Phase II clinical trial of myopia control treatment has enrolled a total of 140 participants across sites in the United States and Taiwan. As of May 29, 50% subjects of this trial has successfully completed the one-year treatment protocol and the remaining 50% subjects are scheduled to complete all treatment by December 2026. The study is scheduled for unblinding in the first quarter of 2027.

Sunhawk Vision Announces SHJ002 Phase 2 DED Results in NIH-Indexed Clinical Therapeutics: Breakthrough Efficacy in Corneal Repair to Redefine Global Market Landscape

The Phase II clinical trial of myopia control treatment has enrolled a total of 140 participants across sites in the United States and Taiwan. As of April 2, 25 subjects have successfully completed the one-year treatment protocol. The study is scheduled for unblinding in the first quarter of 2027.

The company has successfully completed the interim review by the Data Monitoring Committee (DMC) for its Phase II clinical trial of childhood myopia treatment.

FDA approved the Phase-III clinical trial for Dry Eye Disease.

Sunhawk Vision received the approval of Australia patent for the company’s novel eye drops, SHJ002, in treating ocular surface diseases (including dry eye disease).

Sunhawk Vision submitted the request to U.S. FDA for Orphan Drug Designation (ODD) for SHJ002 ophthalmic solution in treating recurrent corneal erosion in patients with Sjogren’s syndrome.

The eye drop SHJ002 for the treatment of dry eye disease has completed the submission of the Investigational New Drug (IND) application for phaseIII clinical trials to the U.S. FDA.

Sunhawk Vision received the approval of Japanese patent for the company’s novel eye drops, SHJ002, in treating ocular surface diseases (including dry eye disease).

Sunhawk Vision Mandated by Global Mega-Pharma Titans for Exclusive One-on-One Closed-Door Summits at BIO 2026 to Leverage Strategic Licensing and Equity Bids for SHJ002 Platform.

The Phase II clinical trial of myopia control treatment has enrolled a total of 140 participants across sites in the United States and Taiwan. As of May 29, 50% subjects of this trial has successfully completed the one-year treatment protocol and the remaining 50% subjects are scheduled to complete all treatment by December 2026. The study is scheduled for unblinding in the first quarter of 2027.

Sunhawk Vision Announces SHJ002 Phase 2 DED Results in NIH-Indexed Clinical Therapeutics: Breakthrough Efficacy in Corneal Repair to Redefine Global Market Landscape

The Phase II clinical trial of myopia control treatment has enrolled a total of 140 participants across sites in the United States and Taiwan. As of April 2, 25 subjects have successfully completed the one-year treatment protocol. The study is scheduled for unblinding in the first quarter of 2027.

The company has successfully completed the interim review by the Data Monitoring Committee (DMC) for its Phase II clinical trial of childhood myopia treatment.

FDA approved the Phase-III clinical trial for Dry Eye Disease.

Sunhawk Vision received the approval of Australia patent for the company’s novel eye drops, SHJ002, in treating ocular surface diseases (including dry eye disease).

Sunhawk Vision submitted the request to U.S. FDA for Orphan Drug Designation (ODD) for SHJ002 ophthalmic solution in treating recurrent corneal erosion in patients with Sjogren’s syndrome.

The eye drop SHJ002 for the treatment of dry eye disease has completed the submission of the Investigational New Drug (IND) application for phaseIII clinical trials to the U.S. FDA.

Sunhawk Vision received the approval of Japanese patent for the company’s novel eye drops, SHJ002, in treating ocular surface diseases (including dry eye disease).

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2022 Taipei Biotech Award.

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