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NCT06969001
Clinical Study for the Evaluation of Safety and Tolerability of SCAI-005 Eye Drops
Phase 1 trial testing SCAI-005 0.04% or placebo in Wet Age Related Macular Degeneration in 48 participants. Completed in 4 September 2025.
4 September 2025
Quick facts
| Lead sponsor | SCAI Therapeutics |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | sequential |
| Masking | double |
| Primary purpose | other |
| Enrollment | 48 |
| Start date | 29 May 2025 |
| Primary completion | 4 September 2025 |
| Estimated completion | 4 September 2025 |
| Sites | 1 location across South Korea |
Drugs / interventions tested
- SCAI-005 0.04% or placebo — full drug profile →
- SCAI-005 0.08% or placebo — full drug profile →
- SCAI-005 0.08% or placebo 2drops — full drug profile →
Conditions studied
- Wet Age Related Macular Degeneration — all drugs for Wet Age Related Macular Degeneration →
Sponsor
SCAI Therapeutics — full company profile →
Who can join
Adults 19 to 50, any sex, with Wet Age Related Macular Degeneration. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
To assess the single-dose and multiple-dose pharmacokinetics (PK), safety and tolerability of SCAI-005 eyedrops(axitinib) in healthy volunteers
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT06969001
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Wet Age Related Macular Degeneration
Currently open trials in the same condition.
- NCT06704009 — NT-101 Topical Ophthalmic Solution in Patients With Wet AMD · Phase 1, PHASE2 · active not recruiting
Other SCAI Therapeutics trials
Trials by the same sponsor.
- NCT05733624 — Clinical Trial to Evaluate the Safety and Efficacy of SCAI-001 Compared to Restasis · Phase 2 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06969001 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by SCAI Therapeutics
- Last refreshed: 9 September 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06969001.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing