Drugs / IBIO-600
last change Jun 2026 re-read 3 minutes ago

IBIO-600

Developed for
obesity disorder
Investigated by
iBio, Inc.

Trials 1

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT07487376 May 2026 → May 2027 expected obesity disorder iBio, Inc. Recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 3

DateIssuerRelease
2026-05-12 iBio, Inc. Regulatory iBio Reports Q3 Fiscal Year 2026 Financial Results and Provides Corporate Update ibioinc.com ↗
2026-04-08 iBio, Inc. Regulatory iBio Received Regulatory Clearance to Initiate Its Phase 1 Clinical Trial of IBIO-600 in Australia ibioinc.com ↗
today announced IBIO-600 has received Clinical Trial Notification (CTN) acknowledgement from Australia’s Therapeutic Goods Administration (TGA) and ethics approval from a Human Research Ethics Committee (HREC), enabling the initiation of a first-in-human clinical trial of IBIO-600 in Australia.
2025-04-07 iBio, Inc. Results iBio Announces IBIO-600 Non-Human Primate Data Showing Extended Half-Life and Muscle Growth, and Interim In Vivo Results for First-in-Class Activin E Antibody, Advancing Cardiometabolic and Obesity Pipeline ibioinc.com ↗
Non-human primate pharmacokinetics data suggests IBIO-600, a potentially best-in-class long-acting anti-myostatin antibody, could have a human half-life as long as 130 days

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 IBIO-600 ClinicalTrials.gov intervention name — accepted as the source's own label NCT07487376 ↗
Route Subcutaneous “IBIO-600 Subcutaneous injection” NCT07487376 ↗