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Nuvectis Pharma Announces Proposed Public Offering of Common Stock

Key Takeaway: Nuvectis Pharma has announced a proposed underwritten public offering of its common stock to raise funds for its drug development programs. The company plans to grant underwriters a 30-day option to purchase additional shares. Proceeds will be used to support clinical trials of its drug candidates NXP800 and NXP900, alongside other corporate needs. The offering is contingent upon market conditions, with no guarantee on its timing or success.

Market Sentiment Analysis

POSITIVE FACTORS

  • Nuvectis Pharma is advancing development programs for NXP800 and NXP900.
  • The public offering provides financial support for hiring and operational growth.
  • The company focuses on developing precision medicines for serious oncology conditions.

CONCERNS & RISKS

  • The offering is subject to market conditions and there’s uncertainty about its completion.
  • There are inherent risks associated with clinical trial outcomes for NXP800 and NXP900.

Full Press Release Details

Nuvectis Pharma Announces Proposed Public Offering
FORT LEE, NJ, February 4, 2025 - Nuvectis
Pharma, Inc. (Nasdaq: NVCT), a clinical-stage biopharmaceutical company focused on the development of innovative precision medicines
for the treatment of serious conditions of unmet medical need in oncology, today announced that it has commenced an underwritten public
offering of its common stock. All of the shares to be sold in the offering will be offered by Nuvectis. In addition, Nuvectis intends
to grant the underwriters a 30-day option to purchase up to an additional 15% of the shares of its common stock offered in the public
offering. The offering is subject to market and other 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.
Lucid Capital Markets is acting as sole book
runner for the offering.
Nuvectis intends to use the net proceeds from
this offering to continue to advance the development programs of NXP800 and NXP900 or any future product candidate, hiring of additional
personnel, capital expenditures, costs of operating as a public company and other general corporate purposes.
The securities described above are being offered
by Nuvectis pursuant to its shelf registration statement on Form S-3 (File No. 333-270657) with the U.S. Securities and Exchange
Commission ("SEC") on March 17, 2023 and declared effective by the SEC on March 29, 2023. A preliminary prospectus
supplement and accompanying prospectus relating to the offering will be filed with the SEC and will be available on the SEC's website
at https://www.sec.gov/. Copies of the final prospectus supplement and the accompanying prospectus relating to these securities may also
be obtained, when available, by contacting Lucid Capital Markets, LLC, 570 Lexington Avenue, 40th floor, New York, NY
The offering of these securities is being made
under an effective shelf registration statement on file with the SEC. 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 under the securities laws of any such state or jurisdiction.
About Nuvectis Pharma
Nuvectis Pharma, Inc. is a biopharmaceutical
company focused on the development of innovative precision medicines for the treatment of serious conditions of unmet medical need in
oncology. The Company is currently developing two clinical-stage drug candidates, NXP800 and NXP900. NXP800 is an oral small molecule
GCN2 activator currently in a Phase 1b clinical trial for the treatment for platinum resistant, ARID1a-mutated ovarian carcinoma and
in an Investigator-sponsored clinical trial for the treatment of cholangiocarcinoma. NXP900 is an oral small molecule inhibitor of the
SRC Family of Kinases (SFK), including SRC and YES1. NXP900 has a unique mechanism of action in that it inhibits both the catalytic and
scaffolding functions of the SRC kinase thereby providing complete shutdown of the signaling pathway. NXP900 is currently in a Phase
1a dose escalation study.
Forward-Looking Statements
This press release contains "forward-looking
statements" within the meaning of the federal securities laws, which statements are subject to substantial risks and uncertainties,
including the risks and uncertainties associated with market conditions and the satisfaction of customary closing conditions related
to the proposed public offering. All statements, other than statements of historical fact, contained in this press release are forward-looking
statements. Forward-looking statements contained in this press release may be identified by the use of words such as "anticipate,"
"believe," "contemplate," "could," "estimate," "expect," "intend,"
"seek," "may," "might," "plan," "potential," "predict," "project,"
"target," "aim," "should," "will," "would," or the negative of these words
or other similar expressions, although not all forward-looking statements contain these words. Forward-looking statements are based on
Nuvectis Pharma, Inc.'s current expectations, including safety and efficacy data generated to date for NXP800 and NXP900, estimates,
and projections about future events and trends that we believe may affect our business, financial condition, results of operations, prospects,
business strategy, and financial needs. The outcome of the events described in these forward-looking statements are subject to inherent
uncertainties, risks, assumptions, market and other conditions, and other factors that are difficult to predict and include statements
and data regarding the preclinical studies for NXP800 and NXP900, and the Phase 1a data for NXP800 and the NXP900 Phase 1a study to date,
as well as the clinical expectations for the ongoing NXP800 Phase 1b study in platinum-resistant, ARID1a-mutated ovarian carcinoma, including
the potential ability of a higher dose intensity going forward in the NXP800 Phase 1b study to generate satisfactory safety and efficacy
results, statements regarding NXP800's potential ability to become a therapeutic option for the treatment of platinum-resistant, ARID1a-mutated
ovarian carcinoma, cholangiocarcinoma, and potentially other cancer indications, and the timing for completion of the clinical trials,
including the ongoing NXP800 investigator-initiated study in cholangiocarcinoma and statements regarding NXP900's therapeutic potential
and the expected timing for the start of the NXP900 Phase 1b program. Further, certain forward-looking statements are based on assumptions
as to future events that may not prove to be accurate. These and other risks and uncertainties are subject to market and other conditions
and described more fully in the section titled "Risk Factors" in our 3Q 2024 Form 10-Q and our other public filings
with the Securities and Exchange Commission ("SEC"). However, these risks are not exhaustive and new risks and uncertainties
emerge from time to time, and it is not possible for us to predict all risks and uncertainties that could have an impact on the forward-looking
statements contained in this press release or other filings with the SEC. Any forward-looking statements contained in this press release
speak only as of the date of this press release. We expressly disclaim any obligation or undertaking to release publicly any updates
or revisions to any forward-looking statements contained herein to reflect any change in our expectations or any changes in events, conditions
or circumstances on which any such statement is based, except as may be required by law, and we claim the protection of the safe harbor
for forward-looking statements contained in the Private Securities Litigation Reform Act of 1995.
Chairman, Chief Executive Officer and President
Media Relations Contact
Christopher M. Calabrese

Frequently Asked Questions

What is Nuvectis Pharma's public offering about?

Nuvectis Pharma has announced an underwritten public offering of its common stock.

How will Nuvectis use the offering proceeds?

The proceeds will advance development programs, hire personnel, and cover corporate costs.

Which two drug candidates is Nuvectis currently developing?

Nuvectis is developing NXP800 and NXP900 for serious oncology conditions.

What market conditions affect the public offering?

The offering's completion depends on market conditions and other factors.

Who is the sole book runner for the offering?

Lucid Capital Markets is acting as the sole book runner for the offering.

Last updated: Feb 4, 2025