AP303
/ Alebund
- LARVOL DELTA
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October 30, 2024
A Study to Evaluate the Safety, Tolerability, PK and PD of AP303 in DKD Patients
(clinicaltrials.gov)
- P1 | N=18 | Not yet recruiting | Sponsor: Alebund Pharmaceuticals
New P1 trial • Diabetic Nephropathy • Nephrology • Renal Disease
May 31, 2024
A Study to Evaluate the Safety, Tolerability, PK and PD of AP303 in Healthy Chinese Participants
(clinicaltrials.gov)
- P1 | N=18 | Completed | Sponsor: Alebund Pharmaceuticals | Not yet recruiting ➔ Completed
Trial completion
March 29, 2024
Alebund's Innovative Investigational Drug AP303 Receives FDA Orphan Drug Designation (ODD) for the Treatment of Autosomal Dominant Polycystic Kidney Disease (ADPKD)
(PRNewswire)
- "Alebund Pharmaceuticals...announced today that the US Food and Drug Administration (FDA) has granted Orphan Drug Designation (ODD) to AP303 for the treatment of autosomal dominant polycystic kidney disease (ADPKD)....This Orphan Drug Designation reflects the need for more new treatment options and the potential for AP303 to address the pressing needs of people living with ADPKD."
Orphan drug • Autosomal Dominant Polycystic Kidney Disease • Polycystic Kidney Disease • Renal Disease
March 13, 2024
A Study to Evaluate the Safety, Tolerability, PK and PD of AP303 in Healthy Chinese Participants
(clinicaltrials.gov)
- P1 | N=18 | Not yet recruiting | Sponsor: Alebund Pharmaceuticals
New P1 trial
July 14, 2023
A Safety, Tolerability, and Pharmacokinetics Study of AP303 in Healthy Subjects
(clinicaltrials.gov)
- P1 | N=62 | Completed | Sponsor: Alebund Pty Ltd | Recruiting ➔ Completed
Trial completion
December 14, 2022
A Safety, Tolerability, and Pharmacokinetics Study of AP303 in Healthy Subjects
(clinicaltrials.gov)
- P1 | N=62 | Recruiting | Sponsor: Alebund Pty Ltd | Not yet recruiting ➔ Recruiting
Enrollment open
August 17, 2022
A Safety, Tolerability, and Pharmacokinetics Study of AP303 in Healthy Subjects
(clinicaltrials.gov)
- P1 | N=62 | Not yet recruiting | Sponsor: Alebund Pty Ltd
New P1 trial
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