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Belite Bio Announces Proposed Underwritten Public Offering of American Depositary Shares

Key Takeaway: Belite Bio announced a proposed underwritten public offering of American Depositary Shares (ADSs) to raise funds for various corporate purposes. The company intends to use the net proceeds to support commercialization efforts, expand its pipeline, and for general working capital. The offering, which is subject to market conditions, allows underwriters a 30-day option to purchase additional ADSs. Belite's lead candidate, Tinlarebant, has completed a Phase 3 trial and is currently involved in ongoing clinical evaluations.

Market Sentiment Analysis

POSITIVE FACTORS

  • Belite Bio is advancing novel therapeutics for unmet medical needs in retinal diseases.
  • The proposed public offering aims to fund important aspects like commercialization and pipeline development.
  • Belite's lead candidate, Tinlarebant, has shown promising results in Phase 3 trials.

CONCERNS & RISKS

  • The offering is subject to market conditions and there is uncertainty about its completion and terms.
  • No assurances are provided regarding the safety and efficacy of drug candidates, which may impact future development.
  • Forward-looking statements indicate potential risks in achieving desired outcomes for clinical trials.

Full Press Release Details

Belite Bio Announces Proposed Underwritten Public
Offering of American Depositary Shares
SAN DIEGO, December 1, 2025 -- Belite
Bio, Inc (NASDAQ: BLTE) ("Belite Bio" or the "Company"), a clinical-stage drug development company focused
on advancing novel therapeutics targeting degenerative retinal diseases that have significant unmet medical needs, today announced that
it has commenced an underwritten public offering of American Depositary Shares ("ADSs"), each representing one of its ordinary
shares. All of the securities in the offering are to be sold by Belite Bio. In addition, Belite Bio intends to grant the underwriters a 30-day option to purchase additional ADSs at the public offering price, less
underwriting discounts and commission. The offering is subject to market conditions, and there can
be no assurance as to whether or when the offering may be completed, or as to the actual size or terms of the offering.
Belite Bio intends to use the net proceeds
of the offering for (i) commercialization preparation, including building our in-house commercialization team, establishing sales
network and systems, and preparing for the commercial manufacture of our future products, if approved, (ii) development and expansion
of pipelines, and (iii) working capital and other general corporate purposes.
Morgan Stanley & Co. LLC, Leerink
Partners, BofA Securities and Cantor are acting as joint active book-running managers for the offering.
This proposed offering will be made only by means of a prospectus
supplement and accompanying prospectus included in Belite's registration statement on Form F-3ASR (File No. 333-284521),
which became effective automatically on January 27, 2025. Copies of the preliminary prospectus supplement and the accompanying prospectus
may be obtained, when available, by visiting EDGAR on the U.S. Securities and Exchange Commission ("SEC") website at www.sec.gov
or from Morgan Stanley & Co. LLC, Attention: Prospectus Department, 180 Varick Street, 2nd Floor, New York, New York 10014 or
by email at prospectus@morganstanley.com; Leerink Partners LLC, Syndicate Department, 53 State Street, 40th Floor, Boston, Massachusetts
02109, by telephone at (800) 808-7525 ext. 6105, or by email at syndicate@leerink.com; BofA Securities, Attention: Prospectus
Department, NC1-022-02-25, 201 North Tryon Street, Charlotte, North Carolina 28255-0001, or by email at dg.prospectus_requests@bofa.com;
or Cantor Fitzgerald & Co., Attention: Equity Capital Markets, 110 E. 59th Street, 6th Floor, New York, New York 10022, or by email
A registration statement relating to these securities has been filed
with the SEC and has become automatically effective. This press release shall not constitute an offer to sell or the solicitation of an
offer to buy, nor shall there be any sale of, these securities in any state or jurisdiction in which such offer, solicitation or sale
would be unlawful prior to registration or qualification of these securities under the securities laws of any such state or jurisdiction.
Belite Bio is a clinical-stage drug development company focused on
advancing novel therapeutics targeting degenerative retinal diseases that have significant unmet medical need, such as Stargardt disease
type 1 (STGD1) and geographic atrophy (GA) in advanced dry age-related macular degeneration (AMD), in addition to specific metabolic diseases.
Belite's lead candidate, Tinlarebant, an oral therapy intended to reduce the accumulation of bisretinoid toxins in the eye, has
completed a Phase 3 trial (DRAGON) in adolescent STGD1 subjects and is currently being evaluated in a Phase 2/3 trial (DRAGON II) in adolescent
STGD1 subjects and a Phase 3 trial (PHOENIX) in subjects with GA.
Important Cautions Regarding Forward Looking Statements
This press release contains forward-looking statements, including
statements about the terms of the proposed public offering, including our expectations with respect to granting the underwriters a 30-day option to purchase
additional ADSs, and the completion, timing and size of the proposed public offering, as
well as any statements regarding matters that are not historical facts, and any other statements containing the words "expect",
"will", "believe", "target", and other similar expressions. No assurance can be given that the proposed
public offering will be completed on the terms described. Completion of the proposed public offering and the terms thereof are subject
to numerous factors, many of which are beyond the control of Belite Bio, including, without limitation, market conditions, failure of
customary closing conditions and the risk factors and other matters set forth in the prospectus supplement and accompanying prospectus
included in the registration statement. Actual results may also differ materially from those indicated in the forward-looking statements
as a result of various important factors related to Belite Bio's business, including but not limited to Belite Bio's ability
to demonstrate the safety and efficacy of its drug candidates; the clinical results for its drug candidates, which may not support further
development or regulatory approval; expectations for the timing of initiation, enrollment and completion of, and data relating to, its
clinical trials; the content and timing of decisions made by the relevant regulatory authorities regarding regulatory approval of Belite
Bio's drug candidates; the potential efficacy of Tinlarebant, as well as those risks more fully discussed in the "Risk Factors"
section in Belite Bio's filings with the U.S. Securities and Exchange Commission. All forward-looking statements are based on information
currently available to Belite Bio, and Belite Bio undertakes no obligation to publicly update or revise any forward-looking statements,
whether as a result of new information, future events or otherwise, except as may be required by law.
Media and Investor Relations Contact:
Jennifer Wu /ir@belitebio.com

Frequently Asked Questions

What is Belite Bio's primary focus?

Belite Bio specializes in developing novel therapeutics for degenerative retinal diseases.

What is the purpose of the public offering?

The proceeds will support commercialization efforts, pipeline expansion, and general corporate needs.

Who is managing the underwritten public offering?

Morgan Stanley, Leerink Partners, BofA Securities, and Cantor are the joint managers.

What is Tinlarebant designed to treat?

Tinlarebant aims to reduce toxic accumulation in the eyes for certain retinal diseases.

How can I access the prospectus for the offering?

The prospectus can be accessed via the SEC website or through the underwriters.

Last updated: Dec 1, 2025