STOCK TITAN

NewcelX signs $1.55M private placement agreements

NewcelX intends to combine proceeds with cash and its previously announced $25 million equity line for NCEL-101 development and planned 2027 trial preparations.

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(Moderate)

Sentiment and the balance of points

Rhea-AI Sentiment reads the wording of the document, how positive or negative its language is on a 1 to 5 scale. The balance of points shown with the takes weighs what the document actually discloses, so the two can disagree, for example when a trial that missed its main goal is described in upbeat language.

Form Type
6-K

Rhea-AI Filing Summary

NewcelX Ltd. (NCEL) entered into securities purchase agreements for a $1.55 million private placement of 471,125 common shares at $3.29 per share, plus warrants to purchase 353,344 common shares at $3.75 per share. The share price is a 20% premium to the November 6, 2026 closing price; the warrant exercise price is 137% of that closing price. The offering includes existing shareholders and is expected to close on or about November 23, 2026, subject to customary closing conditions.

NewcelX intends to use net proceeds together with current cash and its previously announced $25 million equity line primarily to advance NCEL-101 with Eledon Pharmaceuticals, including an FDA-required IND-enabling toxicology study, cell manufacturing capabilities and preparation for a planned Phase 1/2a trial in 2027, as well as working capital and general corporate purposes. The release identifies a risk that NewcelX’s financial position raises substantial doubt about its ability to continue as a going concern.

0 points · 0 major

How this balance works

Rhea-AI gives every point it takes from this document a weight. Minor counts 1, Moderate 3 and Major 9, so one Major point outweighs several Minor ones. The bar adds up the weights on each side, and when neither side holds more than 65% of the total the balance reads Mixed.

It reads the document as published, with the same rules for every company, and it does not look at what the market expected or at how the stock traded, so a point can be objectively good on a day the stock falls.

Rhea-AI Sentiment measures something else, the tone of the wording.

1 major · 1 point

How the balance works

Positive

  • None.

Negative

  • Major pointNewcelX identifies substantial doubt about its ability to continue as a going concern as a financial-position risk.

Filing Explained

The private-placement shares and warrants are unregistered; they cannot be offered or sold in the United States unless an effective registration statement or an applicable exemption permits it.

Equity financing $1.55 million Private placement announced by NewcelX
Common shares 471,125 shares Shares being sold in the private placement
Purchase price $3.29 per share 20% premium to the November 6, 2026 closing price
Warrant shares 353,344 common shares Shares underlying the warrants
Warrant exercise price $3.75 per share 137% of the November 6, 2026 closing price
Premium to last closing price 20% Purchase price compared with the November 6, 2026 closing price
Warrant exercise price as a percentage of last closing price 137% Compared with the November 6, 2026 closing price
private placement financial
"private placement at a purchase price of $3.29 per share"
A private placement is a sale of securities directly to a selected group of investors, typically institutions or accredited investors, instead of through a public offering. It lets a company raise money faster and with fewer regulatory steps; for existing shareholders it matters because the newly issued shares, often sold at a discount, increase the share count and can dilute their ownership.
warrants financial
"warrants to purchase an aggregate of 353,344 common shares"
Warrants are special documents that give you the right to buy a company's stock at a set price before a certain date. They are often used as a way for companies to attract investors or raise money, and their value can increase if the company's stock price goes up.
IND-enabling toxicology study medical
"initiate the FDA-required IND-enabling toxicology study"
A nonclinical program of toxicology studies conducted to support an Investigational New Drug (IND) application to a regulatory authority. These GLP-compliant studies examine how a candidate drug affects whole animals (usually two species) across a range of doses and durations to identify toxic effects, target organs, dose–response relationships and a no-observed-adverse-effect level (NOAEL); their results are used to set safe starting doses and dosing limits for first-in-human clinical trials. Regulatory agencies prescribe the types, species, durations and endpoints required, so the exact study set (e.g., single- and repeat-dose toxicology, safety pharmacology, genotoxicity, reproductive toxicology) depends on the drug modality and intended human use, and the studies demonstrate risk profile rather than proving a drug is safe.
Phase 1/2a clinical trial medical
"preparations for the planned Phase 1/2a clinical trial in 2027"

FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

What are the terms of NCEL’s private placement?

NewcelX announced a $1.55 million private placement of 471,125 common shares at $3.29 per share and warrants to purchase 353,344 common shares at an exercise price of $3.75 per share.

How does NCEL intend to use the financing proceeds?

NewcelX intends to use net proceeds, together with its current cash and previously announced $25 million equity line, primarily to advance NCEL-101, including an IND-enabling toxicology study, cell manufacturing capabilities and preparation for a planned Phase 1/2a trial in 2027, as well as working capital and general corporate purposes.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 6-K

 

REPORT OF FOREIGN PRIVATE ISSUER

PURSUANT TO RULE 13a-16 OR 15d-16

UNDER THE SECURITIES EXCHANGE ACT OF 1934

 

For the Month of November 2026

 

Commission File Number: 001-39957

 

NEWCELX LTD.

(Translation of registrant’s name into English)

 

Hohstrasse 1
8302 Kloten, Switzerland

(Address of principal executive office)

 

Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F:

 

☒ Form 20-F        ☐ Form 40-F

 

 

 

 

 

 

CONTENTS

 

On November 9, 2026, NewcelX Ltd., a corporation incorporated under the laws of Switzerland (the “Company”), issued a press release titled: “NewcelX Announces Pricing of $1.55 Million Equity Financing at 20% Premium Pricing to Market.” A copy of this press release is furnished herewith as Exhibit 99.1.

 

The first, second, third, fourth, sixth and seventh paragraphs of the press release attached to this Form 6-K as Exhibit 99.1 are incorporated by reference into the Company’s Registration Statements on Form F-3 (File Nos. 333-282788, 333-268690, 333-269220, 333-295770, 333-284811 and 333-298458), filed with the Securities and Exchange Commission, to be a part thereof from the date on which this report is submitted, to the extent not superseded by documents or reports subsequently filed or furnished.

 

1

 

 

EXHIBIT INDEX

 

Exhibit
Number
  Description of Document
99.1   Press release titled: “NewcelX Announces Pricing of $1.55 Million Equity Financing at 20% Premium Pricing to Market”

 

2

 

 

SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

 

  NewcelX Ltd.
     
Date: November 9, 2026 By: /s/ Ronen Twito
    Name: Ronen Twito
    Title: Chief Executive Officer

 

3

 

Exhibit 99.1 

 

NewcelX Announces Pricing of $1.55 Million Equity Financing at 20% Premium Pricing to Market

 

The financing led by international healthcare investors, alongside The Crushing
T1 Foundation, reinforces confidence in NewcelX’s strategy and long-term potential

 

ZURICH, Switzerland, November 9, 2026 (GLOBE NEWSWIRE) -- NewcelX Ltd. (Nasdaq: NCEL), a clinical-stage biopharmaceutical company developing stem cell-based therapies for type 1 diabetes, today announced that it has entered into securities purchase agreements for a private placement at a purchase price of $3.29 per share, representing a 20% premium to the last closing price of the Company’s common shares on November 6, 2026.

 

Pursuant to the terms of the securities purchase agreements, the Company is selling an aggregate of 471,125 common shares and one series of warrants to purchase an aggregate of 353,344 common shares at an exercise price of $3.75 per share, which is 137% of the last closing price of the Company’s common shares on November 6, 2026.

 

The offering includes participation from existing shareholders and is expected to close on or about November 23, 2026, subject to the satisfaction of customary closing conditions.

 

The Company intends to use the net proceeds from the offering, together with its current cash position, and previously announced $25 million equity line, primarily to advance NCEL-101, NewcelX’s lead program for type 1 diabetes, in collaboration with Eledon Pharmaceuticals, and specifically to initiate the FDA-required IND-enabling toxicology study, advance cell manufacturing capabilities and support preparations for the planned Phase 1/2a clinical trial in 2027, and for working capital and general corporate purposes.

 

“We are pleased to welcome this distinguished group of healthcare investors, whose experience, reputation, and long-term perspective bring significant value beyond their financial investment,” said Ronen Twito, CEO & Executive Chairman of NewcelX. “We believe that their participation, together with involvement of The Crushing T1 Foundation, represents a strong vote of confidence in our technology, strategy, and clinical potential. Importantly, the investment at a substantial premium to the prevailing market price underscores the conviction of these investors in the long-term value of NewcelX. This financing comes at an important stage as we advance toward initiating our IND-enabling studies following our successful Pre-IND meeting with the FDA and prepare for our planned Phase 1/2a clinical trial in 2027, in collaboration with Eledon Pharmaceuticals.”

 

The securities described above are being issued in a private placement under Section 4(a)(2) of the Securities Act of 1933, as amended (the “Securities Act”), and Regulation D promulgated thereunder and have not been registered under the Securities Act, or applicable state securities laws. Accordingly, the securities may not be offered or sold in the United States except pursuant to an effective registration statement or an applicable exemption from the registration requirements of the Securities Act and such applicable state securities laws.

 

 

 

 

This press release does not constitute an offer to sell or a solicitation of an offer to buy the securities in this offering, nor shall there be any sale of these securities in any state or other jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration or qualification under the securities laws of any such state or other jurisdiction.

 

About NewcelX

 

NewcelX is an innovative biopharmaceutical company focused on developing transformative stem-cell-derived therapies for Type 1 Diabetes. Built on a validated human pluripotent stem cell (hPSC) platform, the Company’s lead program, NCEL-101, is designed to restore functional insulin production through scalable, off-the-shelf cell replacement. NewcelX is advancing a comprehensive therapeutic approach for Type 1 Diabetes integrating cell therapy, immune protection, and translational science to address critical unmet medical needs.

 

Social Media: LinkedIn, Facebook, X, Instagram

 

Website: www.newcelx.com 

 

Forward-Looking Statements

 

This press release contains expressed or implied forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 and other applicable securities laws. For example, NewcelX is using forward-looking statements when it discusses the timing and completion of the offering, the satisfaction of customary closing conditions related to the offering, the intended use of proceeds therefrom, the advancement and development of NCEL-101, the initiation and timing of IND-enabling studies, its manufacturing capabilities and scalability, and the timing and commencement of its planned Phase 1/2a clinical trial, including its plans to commence such trial in 2027. These forward-looking statements and their implications are based on the current expectations of the management of NewcelX and are subject to a number of factors and uncertainties that could cause actual results to differ materially from those described in the forward-looking statements. The following factors, among others, could cause actual results to differ materially from those described in the forward-looking statements: the regulatory pathways that NewcelX may elect to utilize in seeking European Medicines Agency, the FDA, and other regulatory approvals; its ability to drive revenue growth, enhance research and development capabilities, and improve financial performance is subject to uncertainties; that its financial position raises substantial doubt about its ability to continue as a going concern; its ability to maintain listing and effectively comply with the listing requirements of the Nasdaq; changes in technology and market requirements; potential delays or obstacles in launching or completing clinical trials, including its expectations regarding the timing of commencing further clinical trials, the process entailed in conducting each such trial, including dosages, and the order of such trials with each of its product candidates or whether such trials will be conducted at all; competitive companies, technologies and its industry; the development and commercialization, if any, of any other product candidates that it may seek to develop; products that may not be approved by regulatory agencies; technologies that may not be validated or accepted by the scientific community; the inability to retain or attract key employees; unforeseen scientific difficulties with products in development; the scope of protection it is able to establish and maintain for intellectual property rights covering its product candidates and its ability to operate its business without infringing the intellectual property rights of others; higher-than-expected product costs; results in the laboratory that do not translate to clinical success; insufficient patent protection; possible adverse safety outcomes; its ability to establish and maintain strategic partnerships and other corporate collaborations; risks related to changes in healthcare laws, rules and regulations in the United States or elsewhere; delays in developing or introducing new technologies, products, or applications; competitive pressures that could reduce market share or pricing; the overall global political and economic environment in the countries in which we operate; and security, political and economic instability in the Middle East that could harm its business, including due to the current security situation in Israel. Except as otherwise required by law, NewcelX does not undertake any obligation to publicly release revisions to these forward-looking statements to reflect events or circumstances after the date hereof or to reflect the occurrence of unanticipated events. More detailed information about the risks and uncertainties affecting the Company is contained under the heading “Risk Factors” in its Annual Report on Form 20-F for the year ended December 31, 2025, filed with the U.S. Securities and Exchange Commission (“SEC”) and available at www.sec.gov, as well as in subsequent filings made by NewcelX.

 

Investor Contact

 

KCSA Strategic Communications
Valter Pinto, Managing Director
PH: (212) 896-1254
NewCelX@kcsa.com

 

Company Contact

 

Sarah Bazak
InvestorRelations@newcelx.com

 

 

 

Filing Exhibits & Attachments

1 document

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