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SUNHAWKVISION Expands Core Technology Platform to Prevent and Treat Ocular Toxicities Induced by ADC Anticancer Drugs, Filing U.S. Patent to Secure Global Strategic IP Position

The Phase II clinical trial of myopia control treatment has enrolled a total of 112 participants. Approximately 80% of the subjects have successfully completed one year of the trial. The last subject is expected to complete the study medication administration by December 31, 2026, marking the completion of the treatment phase. The trial is progressing smoothly and in line with expectations.

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.

SUNHAWKVISION Expands Core Technology Platform to Prevent and Treat Ocular Toxicities Induced by ADC Anticancer Drugs, Filing U.S. Patent to Secure Global Strategic IP Position

The Phase II clinical trial of myopia control treatment has enrolled a total of 112 participants. Approximately 80% of the subjects have successfully completed one year of the trial. The last subject is expected to complete the study medication administration by December 31, 2026, marking the completion of the treatment phase. The trial is progressing smoothly and in line with expectations.

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.

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