New eye drops aim to soothe dry eyes in major trial
NCT ID NCT06717152
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This Phase 3 study tested SJP-0132 eye drops against placebo in 427 Chinese adults with dry eye disease. Participants used the drops four times daily for 8 weeks. The goal was to see if the drops improve eye surface damage and reduce dryness symptoms.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- SJP-0132 eye drops
- What this could lead to
- If successful, SJP-0132 could offer a new treatment option to relieve dry eye symptoms and improve eye surface health.
- What could go wrong
- This is a completed Phase 3 trial, but results are not yet published. The benefit over placebo may be modest, and individual responses can vary.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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427 people
The number who actually took part.
- Started
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Dec 2024
- Finished
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Sep 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 70 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Male or female patients aged between 18 and 70 at the time of the informed consent * Outpatient patients * The patient's self-described dry eye symptom is more than 6 months or has the clinical diagnosis certificate of dry eye in the past 6 months at the time of the informed consent * Tear film break-up time of \<= 5 seconds at the beginning of screening and treatment period Exclusion Criteria: * Patients who have previously used SJP-0132 eye drops * Patients who participated in or are currently participating in or planned to participate in other clinical studies within three months prior to the start of the screening period * Patients who plan to wear corneal contact lenses between the beginning of the screening period and the end of the treatment period * Patients who have undergone eye surgery (including laser surgery) or planned to undergo any eye surgery during the study period within one year prior to the beginning of the corneal transplantation surgery or screening period * Any ophthalmic disease except for the dry eye (including eyeball or periocular infection, allergic or proliferative eye disease) is present at the beginning of the screening period and at the beginning of the treatment period. However, it does not include chronic eye disease patients who do not need treatment and may not become worse before the end of the treatment period * Have known history of hypersensitivity or serious adverse reaction to any of the study drug ingredients * Patients suffering from serious cardiovascular, respiratory, endocrine, digestive, urinary, blood, neurological, mental, ocular or peripheral malignancies (cured in or at the beginning of the screening period but not exceeding five years), at the beginning of screening and treatment period * A patient at the beginning of screening and at treatment period who has a positive blood serum pregnancy test result or is in lactation, or a female patient who has planned pregnancy during the study period or has fertility but is unable to use effective contraception during the study period, or a female partner of a male patient who is unable to use effective contraception during the study * Patients identified at the beginning of screening and treatment period as researchers, research coordinators, researchers and immediate relatives of the persons referred to above * At the beginning of the screening and treatment period, investigators determine that patients who were unable to comply with the requirements of the program or were unable to come to hospital on schedule (e.g. patients who planned to travel or stay in the field during the period prior to the end of the treatment period) * At the beginning of the screening and treatment period, investigators decide that the patients who were not suitable for the trial were not suitable for the other reasons * Meet the other protocol-specified exclusion criteria
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Affiliated Eye Hospital of Nanchang University
Nanchang, Jiangxi, China
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Affiliated Hospital of Zunyi Medical University
Zunyi, Guizhou, China
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Beijing Hospital
Beijing, Beijing Municipality, China
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Beijing Tongren Hospital
Beijing, Beijing Municipality, China
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Dalian No.3 People's Hospital
Dalian, Liaoning, China
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Eye & ENT Hospital of Fudan University
Shanghai, Shanghai Municipality, China
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Eye Hospital, WMU
Wenzhou, Zhejiang, China
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Henan Eye Hospital
Zhengzhou, Henan, China
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Joint Shantou International Eye Center of Shantou University and the Chinese University of Hong Kong
Shantou, Guangdong, China
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Longhua Hospital Shanghai University of Traditional Chinese Medicine
Shanghai, Shanghai Municipality, China
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Ningbo Eye Hospital
Ningbo, Zhejiang, China
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Peking Union Medical College Hospital
Beijing, Beijing Municipality, China
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Peking University Shenzhen Hospital
Shenzhen, Guangdong, China
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People's Hospital of Hunan Province
Changsha, Hunan, China
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Renmin Hospital of Wuhan University
Wuhan, Hubei, China
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Shandong Eye Hospital
Jinan, Shandong, China
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Shanxi Eye Hospital
Taiyuan, Shanxi, China
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Shenzhen People's Hospital
Shenzhen, Guangdong, China
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The Affiliated Hospital of Guizhou Medical University
Guiyang, Guizhou, China
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The First Affiliated Hospital of University of South China
Hengyang, Hunan, China
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The First Affiliated Hospital of Xi'an Jiaotong University
Xi'an, Shaanxi, China
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The First Affiliated Hospital of Zhengzhou University
Zhengzhou, Henan, China
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The First Bethune Hospital of Jilin University
Changchun, Jilin, China
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The Fourth Affiliated Hospital of Soochow University
Suzhou, Jiangsu, China
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The Fourth People's Hospital of Shenyang
Shenyang, Liaoning, China
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The Second Norman Bethune Hospital of Jilin University
Changchun, Jilin, China
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The first people's hospital of Xian Yang
Xianyang, Shanxi, China
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Tianjin Medical University Ophthalmology Hospital
Tianjin, Tianjin Municipality, China
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Tongji Hospital affiliated to Tongji Medical College of Huazhong University of Science & Technology
Wuhan, Hubei, China
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Union Hospital Tongji Medical College Huazhong University of Science and Technology
Wuhan, Hubei, China
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West China Hospital of Sichuan University
Chengdu, Sichuan, China
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Xiamen Eye Center of Xiamen University
Xiamen, Fujian, China
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Xiangya Hospital Central South University
Changsha, Hunan, China
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Zhejiang Provincial People's Hospital
Hangzhou, Zhejiang, China
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Zhongshan Ophthalmic Center, Sun Yat-sen University
Guangzhou, Guangdong, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a thymosin beta 4 eye drop soothe dry eye?
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- Can four eye scanners detect how miebo stabilizes tears?