A Study of STSP-0902 Ophthalmic Solution in Healthy Subjects

NCT ID: NCT06597422

Last Updated: 2025-01-20

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE1
• Total Enrollment: 80 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-10-20
• Study Completion Date: 2025-05-31

Brief Summary

This trial is a Phase I clinical study to evaluate the safety, tolerability, and pharmacokinetic (PK) characteristics of STSP-0902 ophthalmic solution in healthy subjects following single and multiple administrations. The study plans to enroll 80 healthy subjects and is divided into three stages: the single-dose study stage, the multiple-dose study stage, and the tear PK study stage. The single-dose and multiple-dose study stages are randomized, double-blind, placebo-controlled, dose-escalation designs, while the tear PK study stage is a single-dose, open-label design.

Conditions

Neurotrophic Keratitis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Single Low Dose Arm

Low dose of STSP-0902 ophthalmic solution to study eye. Single dose.

Group Type: EXPERIMENTAL

STSP-0902 ophthalmic solution

Intervention Type: DRUG

Eye drop, single dose

Single Middle Dose Arm

Middle dose of STSP-0902 ophthalmic solution to study eye. Single dose.

Group Type: EXPERIMENTAL

STSP-0902 ophthalmic solution

Intervention Type: DRUG

Eye drop, single dose

Single High Dose Arm

High dose of STSP-0902 ophthalmic solution to study eye. Single dose.

Group Type: EXPERIMENTAL

STSP-0902 ophthalmic solution

Intervention Type: DRUG

Eye drop, single dose

Single Control Dose Arm

STSP-0902 Placebo to study eye. Single dose.

Group Type: EXPERIMENTAL

STSP-0902 Placebo

Intervention Type: DRUG

Eye drop, single dose

Multiple Low Dose Arm

Low dose of STSP-0902 ophthalmic solution to study eye. Three times daily for a total of 8 days.

Group Type: EXPERIMENTAL

STSP-0902 ophthalmic solution

Intervention Type: DRUG

Eye drop, three times daily for a total of 8 days

Multiple Middle Dose Arm

Middle dose of STSP-0902 ophthalmic solution to study eye. Three times daily for a total of 8 days.

Group Type: EXPERIMENTAL

STSP-0902 ophthalmic solution

Intervention Type: DRUG

Eye drop, three times daily for a total of 8 days

Multiple High Dose Arm

High dose of STSP-0902 ophthalmic solution to study eye. Three times daily for a total of 8 days.

Group Type: EXPERIMENTAL

STSP-0902 ophthalmic solution

Intervention Type: DRUG

Eye drop, three times daily for a total of 8 days

Multiple Highest Dose Arm

Middle dose of STSP-0902 ophthalmic solution to study eye. Six times daily for a total of 8 days.

Group Type: EXPERIMENTAL

STSP-0902 ophthalmic solution

Intervention Type: DRUG

Eye drop, six times daily for a total of 8 days

Multiple Control Dose Arm

STSP-0902 Placebo to study eye. Multiple doses.

Group Type: EXPERIMENTAL

STSP-0902 Placebo

Intervention Type: DRUG

Eye drop, multiple doses

Tear PK study Arm

STSP-0902 ophthalmic solution to both eyes. Single dose.

Group Type: EXPERIMENTAL

STSP-0902 ophthalmic solution

Intervention Type: DRUG

Eye drop, single dose, tear samples will be collected

Interventions

STSP-0902 ophthalmic solution

Eye drop, single dose

Intervention Type: DRUG

STSP-0902 Placebo

Eye drop, single dose

Intervention Type: DRUG

STSP-0902 ophthalmic solution

Eye drop, three times daily for a total of 8 days

Intervention Type: DRUG

STSP-0902 ophthalmic solution

Eye drop, six times daily for a total of 8 days

Intervention Type: DRUG

STSP-0902 Placebo

Eye drop, multiple doses

Intervention Type: DRUG

STSP-0902 ophthalmic solution

Eye drop, single dose, tear samples will be collected

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Healthy male or female subjects aged between 18 and 45 years (inclusive).

2. Male subjects with a weight of ≥50.0 kg, and female subjects with a weight of ≥45.0 kg, with a Body Mass Index (BMI) between 19.0 and 26.0 kg/m² (inclusive).

3. Both eyes have a corrected visual acuity of ≥1.0, with normal or clinically insignificant results from eye examinations, including slit-lamp examination, intraocular pressure measurement, and fundus examination.

4. Schirmer I test results for both eyes are ≥10 mm/5 minutes (applicable only to subjects in the tear PK study stage).

5. Physical examination, vital signs, 12-lead ECG, chest imaging, and laboratory tests (including hematology, urinalysis, blood chemistry, and coagulation function) are normal or clinically insignificant during the screening period.

6. Subjects (including their partners) agree to use effective non-drug contraception during the trial and for 6 months after the last dose and must not plan to conceive, donate sperm, or donate eggs.

7. Subjects are fully informed about the content, process, and potential adverse effects of the trial, voluntarily sign the informed consent form, and be willing to complete the trial, follow-up, and related examinations according to the trial plan.

Exclusion Criteria

1. History or current presence of any eye disease other than refractive errors (e.g., myopia, hyperopia, astigmatism).

2. History of any eye surgery (including laser correction surgery) or having only one functional eye.

3. Use of any topical eye medication (e.g., artificial tears, traditional Chinese medicine eye drops, antibiotic eye drops, recombinant monoclonal antibody eye drops, eye gels, etc.) within 1 month prior to screening.

4. Wearing contact lenses within 2 weeks before screening or needing to wear contact lenses during the clinical study.

5. Clinically significant abnormal results from corneal fluorescein staining (applicable only to subjects in the single-dose and multiple-dose study stages).

6. History or current presence of any severe systemic disease, including but not limited to cardiovascular, cerebrovascular, respiratory, gastrointestinal, endocrine, metabolic, neurological, hematological, oncological, immune, infectious, or psychiatric disorders, especially those that may affect the eyes (e.g., hypertension, diabetes, hyperthyroidism).

7. Abnormal and clinically significant results in any of the following tests: Hepatitis B surface antigen, Hepatitis C antibody, syphilis-specific antibody, or HIV test.

8. Allergy to any component of the investigational product or excipients, history of allergies (especially eye allergies), or a known history of food or drug allergies.

9. Vaccination within 1 month prior to screening or planned vaccination during the trial.

10. Use of prescription drugs, over-the-counter drugs, or herbal medicines within 2 weeks before screening.

11. History of treatment with nerve growth factor (NGF) drugs (e.g., murine NGF) or use of other neurotrophic drugs (e.g., B vitamins, fish oil, etc.) within 3 months before screening.

12. Underwent any major surgery within 6 months prior to screening or has plans for surgery during the trial.

13. History of smoking within 3 months before screening, defined as smoking more than 5 cigarettes or an equivalent amount of tobacco per day on average, or inability to abstain from any tobacco products during the study.

14. Regular alcohol consumption within 6 months before screening, defined as an average daily alcohol intake of more than 2 units (1 unit = 360 mL of beer, 45 mL of spirits with 40% alcohol, or 150 mL of wine), or a positive alcohol breath test result, or inability to abstain from any alcohol products during the study.

15. Daily consumption of more than 5 cups of coffee or strong tea (each cup ≥150 mL) within 3 months before screening, or inability to abstain during the study.

16. History of drug abuse (e.g., morphine, ketamine, tetrahydrocannabinol [cannabis], methamphetamine, MDMA [ecstasy], cocaine, etc.) or a positive drug abuse screening result.

17. Blood loss or blood donation >400 mL within 3 months prior to screening, or history of blood transfusion within 4 weeks before screening, or plans to donate blood or blood components during the trial or within 3 months after the trial ends.

18. Participation in any clinical trial and receipt of investigational drugs, devices, or vaccines within 3 months before screening.

19. Pregnant or lactating women, those with a positive blood pregnancy test, or women who have not used effective contraception within 2 weeks before screening.

20. Difficulty in administering eye drops, difficulty with venipuncture, inability to tolerate venipuncture for blood sampling, or history of needle phobia or blood phobia.

21. Any other condition that, in the investigator's opinion, makes the subject unsuitable for participation in this trial.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Staidson (Beijing) Biopharmaceuticals Co., Ltd

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Laichun Lu, Ph.D

Role: PRINCIPAL_INVESTIGATOR

Beijing Tongren Hospital

Locations

Beijing Tongren Hospital, Capital Medical University

Beijing, Beijing Municipality, China

Countries

China

Other Identifiers

STSP-0902-02-001

Identifier Type: -

Identifier Source: org_study_id