pdufa.bio

Tinlarebant

Page updated ·next FDA decision on the calendar ·Data as of Nov 5, 2026 9:00 PM ET

Tinlarebant is a Belite Bio, Inc program in stargardt disease type 1 (STGD1). Its PDUFA date is Feb 12, 2027, the FDA's goal date to complete review of the application. Every date links its source.

BLTE catalyst hub

All upcoming FDA decision dates on the 2026 PDUFA calendar

About this program

Indication under review: Stargardt disease type 1 (STGD1). Sponsor: Belite Bio, Inc (BLTE). Market-cap tier at the time we tracked it: Mid. We track 2 catalyst events for this program: 2 upcoming and 0 in the record. A PDUFA date is the FDA's target date to complete review of a marketing application; a readout is the sponsor's expected date for clinical trial results. What a PDUFA date is · why we do not compare trial results across drugs.

Catalyst history

PDUFA · Feb 12, 2027BLTEReadout · Jun 2027BLTE

Specialist biotech funds holding BLTE, 13F for the quarter ended June 30, 2026

FundSharesValue at quarter endFiling
RTW Investments715,332$110.2 millionfiled August 14, 2026
OrbiMed Advisors13,300$2.0 millionfiled August 14, 2026

13F reports list long positions in common stock at quarter end, are due 45 days later, and show no short positions or later trades. Notes, warrants and other instruments are not counted as shares.

Questions

When is Tinlarebant's next FDA decision or readout?

Tinlarebant's PDUFA date is Feb 12, 2027. That is the FDA's goal date to complete review of the application; the agency can act earlier or extend it.

What happened at Tinlarebant's most recent FDA decision?

No FDA decision for Tinlarebant is in our archive yet.

What is Tinlarebant used for?

In our records Tinlarebant is under review or in development for Stargardt disease type 1 (STGD1).

Who makes Tinlarebant?

Belite Bio, Inc (BLTE).

Where does this data come from?

FDA announcements, sponsor press releases and SEC filings; every date on this page links its source.