Drugs / SNP-ACTH (1-39)
last change Jun 2023 re-read 3 minutes ago

SNP-ACTH (1-39)

Developed for
idiopathic membranous glomerulonephritis
Investigated by
Cerium Pharmaceuticals, Inc.

Trials 1

2024202520262027
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 3 NCT05696613 Mar 2023 → Apr 2027 expected idiopathic membranous glomerulonephritis Cerium Pharmaceuticals, Inc. Recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 1

DateIssuerRelease
2023-06-21 Cerium Pharmaceuticals, Inc. Regulatory Cerium Pharmaceuticals receives FDA Orphan Drug Designation for Corticotropin (ACTH) porcine (synthetic) for the treatment of Membranous Nephropathy ceriumpharma.com ↗
Cerium Pharmaceuticals, Inc. announced that the U.S. Food and Drug Administration (FDA) granted orphan drug designation (ODD) for Corticotropin (ACTH) porcine (synthetic), otherwise referred to as SNP-ACTH (1-39) Gel.

All press releases naming this drug 1 release

DateIssuerRelease

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as SNP-ACTH (1-39) ClinicalTrials.gov intervention name — accepted as the source's own label NCT05696613 ↗
Route Subcutaneous “3mg SNP-ACTH Gel subcutaneous (sc) injection 3 times per week” NCT05696613 ↗