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shv_information2025-12-31 15:35:412025-12-31 15:35:41Enrollment of phase-2 myopia control trial (NCT06579287) of Sunhawk vision had successfully completed on December 31, 2025.News
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shv_information2025-12-31 15:35:412025-12-31 15:35:41Enrollment of phase-2 myopia control trial (NCT06579287) of Sunhawk vision had successfully completed on December 31, 2025.
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shv_information2025-12-12 15:27:072025-12-12 15:27:07FDA approved the Phase-III clinical trial for Dry Eye Disease.
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shv_information2025-12-10 15:21:422025-12-10 15:21:42Sunhawk Vision received the approval of Australia patent for the company’s novel eye drops, SHJ002, in treating ocular surface diseases (including dry eye disease).
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shv_information2025-11-03 09:22:522025-11-03 14:00:52Sunhawk 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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shv_information2025-10-07 10:11:232025-10-07 10:11:23The 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.
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shv_information2025-09-22 15:17:222025-09-30 13:06:03Sunhawk 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 has signed a contract with a U.S. pharmaceutical company with 30 years of manufacturing experience and is scheduled to manufacture clinical trial ophthalmic solution in the United States in August 2025.
The first study participant was recruited to the phase-2 myopia control trial.

Preliminary results of Phase II clinical trial evaluating the treatment of corneal erosion in patients with Sjogren’s syndrome
The first study participant was recruited to the phase-2 myopia control trial.

The clinical data on the Phase-II trial for corneal erosion in patients with Sjogren’s syndrome (NCT06381986) were locked on May 5, 2025. The data were unblinded and under statistical analysis.
The first study participant was recruited to the phase-2 myopia control trial.

Sunhawk Vision has completed all subject assessments in its Phase II clinical trial evaluating the treatment of corneal erosion in patients with Sjogren’s syndrome.
The first study participant was recruited to the phase-2 myopia control trial.

Sunhawk Vision has been registration as an Emerging Stock approved by the Taipei Exchange (OTC) Trading Center, meanwhile trading will commence from March 10, 2025.
The first study participant was recruited to the phase-2 myopia control trial.

The first study participant was recruited to the phase-2 myopia control trial.
The first study participant was recruited to the phase-2 myopia control trial.
https://sunhawkvision.com/wp-content/uploads/2025/10/news-scaled.jpg
1862
2560
shv_information
/wp-content/uploads/2024/11/logo-color-new_v2.png
shv_information2025-12-31 15:35:412025-12-31 15:35:41Enrollment of phase-2 myopia control trial (NCT06579287) of Sunhawk vision had successfully completed on December 31, 2025.
https://sunhawkvision.com/wp-content/uploads/2025/10/news-scaled.jpg
1862
2560
shv_information
/wp-content/uploads/2024/11/logo-color-new_v2.png
shv_information2025-12-12 15:27:072025-12-12 15:27:07FDA approved the Phase-III clinical trial for Dry Eye Disease.
https://sunhawkvision.com/wp-content/uploads/2025/10/news-scaled.jpg
1862
2560
shv_information
/wp-content/uploads/2024/11/logo-color-new_v2.png
shv_information2025-12-10 15:21:422025-12-10 15:21:42Sunhawk Vision received the approval of Australia patent for the company’s novel eye drops, SHJ002, in treating ocular surface diseases (including dry eye disease).
https://sunhawkvision.com/wp-content/uploads/2025/10/news-scaled.jpg
1862
2560
shv_information
/wp-content/uploads/2024/11/logo-color-new_v2.png
shv_information2025-11-03 09:22:522025-11-03 14:00:52Sunhawk 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.
https://sunhawkvision.com/wp-content/uploads/2025/10/news-scaled.jpg
1862
2560
shv_information
/wp-content/uploads/2024/11/logo-color-new_v2.png
shv_information2025-10-07 10:11:232025-10-07 10:11:23The 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.
https://sunhawkvision.com/wp-content/uploads/2025/09/yi-sheng-jian-cha-bing-ren-shi-li-scaled.jpg
2560
1703
shv_information
/wp-content/uploads/2024/11/logo-color-new_v2.png
shv_information2025-09-22 15:17:222025-09-30 13:06:03Sunhawk 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 has signed a contract with a U.S. pharmaceutical company with 30 years of manufacturing experience and is scheduled to manufacture clinical trial ophthalmic solution in the United States in August 2025.
The first study participant was recruited to the phase-2 myopia control trial.

Preliminary results of Phase II clinical trial evaluating the treatment of corneal erosion in patients with Sjogren’s syndrome
The first study participant was recruited to the phase-2 myopia control trial.

The clinical data on the Phase-II trial for corneal erosion in patients with Sjogren’s syndrome (NCT06381986) were locked on May 5, 2025. The data were unblinded and under statistical analysis.
The first study participant was recruited to the phase-2 myopia control trial.

Sunhawk Vision has completed all subject assessments in its Phase II clinical trial evaluating the treatment of corneal erosion in patients with Sjogren’s syndrome.
The first study participant was recruited to the phase-2 myopia control trial.

Sunhawk Vision has been registration as an Emerging Stock approved by the Taipei Exchange (OTC) Trading Center, meanwhile trading will commence from March 10, 2025.
The first study participant was recruited to the phase-2 myopia control trial.

The first study participant was recruited to the phase-2 myopia control trial.
The first study participant was recruited to the phase-2 myopia control trial.



Enrollment of phase-2 myopia control trial (NCT06579287) of Sunhawk vision had successfully completed on December 31, 2025.
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 has signed a contract with a U.S. pharmaceutical company with 30 years of manufacturing experience and is scheduled to manufacture clinical trial ophthalmic solution in the United States in August 2025.
Preliminary results of Phase II clinical trial evaluating the treatment of corneal erosion in patients with Sjogren’s syndrome
The clinical data on the Phase-II trial for corneal erosion in patients with Sjogren’s syndrome (NCT06381986) were locked on May 5, 2025. The data were unblinded and under statistical analysis.
Sunhawk Vision has completed all subject assessments in its Phase II clinical trial evaluating the treatment of corneal erosion in patients with Sjogren’s syndrome.