Clinical trial
A Phase I/IIa, Dose Escalation Study Evaluating the Safety, Tolerability, and Preliminary Efficacy of Intraductal Administration of RXRG001 to Parotid Gland(s) in Adults With Radiation-Induced Xerostomia and Hyposalivation
NCT06714253 is registered in ClinicalTrials.gov with RiboX Therapeutics Ltd. as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase I/IIa, Dose Escalation Study Evaluating the Safety, Tolerability, and Preliminary Efficacy of Intraductal Administration of RXRG001 to Parotid Gland(s) in Adults With Radiation-Induced Xerostomia and Hyposalivation
- Lead sponsor
- RiboX Therapeutics Ltd.
- Phase
- Phase 1/2
- Overall status
- Recruiting
- Start date
- March 5, 2025
- Completion date
- August 31, 2027
- Enrollment
- 42 (estimated)
- Sites
- 5
Conditions
As the registry lists them; a condition with its own page is linked.
radiation-induced xerostomia and hyposalivation