STOCK TITAN

XTL Completed the Acquisition of Psyga Bio Ltd.

(Positive)

XTL Biopharmaceuticals (NASDAQ, TASE: XTLB) completed the acquisition of approximately 83.40% of Psyga Bio, transforming XTL into a focused psychedelic medicine company. Operations center on an advanced psilocybin-based clinical pipeline, a licensed GMP-ready manufacturing facility, and a proprietary IP library of over 250 mushroom strains.

The deal was structured via ADS issuance equaling about 33.36% of XTL’s post-transaction capital, plus up to an additional 25.02% tied to three clinical and commercial milestones. A concurrent approved private placement added $1,500,000 in cash to support clinical programs, including three submitted trials and four more planned in Israel.

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Positive

  • Acquisition of ~83.40% of Psyga Bio shares, gaining control of assets
  • Shift to exclusive psychedelic medicine focus with advanced clinical pipeline
  • Ownership of a licensed, GMP-ready psychedelic API manufacturing facility
  • Access to proprietary IP library of 250+ biologically active mushroom strains
  • $1,500,000 cash infusion from approved private placement to fund plans
  • Up to 25.02% additional equity consideration tied to milestone achievements

Negative

  • Equity issuance equal to ~33.36% of post-transaction capital dilutes holders
  • Potential further dilution of up to 25.02% upon milestone achievements

News Market Reaction – XTLB

-8.79% 28.9x vol
15 alerts
-8.79% Session close to close
+46.0% Peak Tracked
-21.5% Trough Tracked
$6.46M Market Cap
28.9x Rel. Volume

In the Jul 1 session, XTLB declined 8.79%, reflecting a notable negative market reaction. Argus tracked a peak move of +46.0% during that session. Argus tracked a trough of -21.5% from its starting point during tracking. Our momentum scanner triggered 15 alerts that day, indicating notable trading interest and price volatility. Trading volume was exceptionally heavy at 28.9x the daily average, suggesting significant selling pressure.

Data tracked by StockTitan Argus on the day of publication.

Market Context

The stock moved -8.8% in the session following this news. A negative reaction despite positive news ...
Analysis

The stock moved -8.8% in the session following this news. A negative reaction despite positive news fits a concern over dilution from the 33.36% initial stake and up to 25.02% milestone equity. Prior acquisitions lifted shares, so pressure would highlight shifting risk perceptions or listing worries.

Key Figures

Psyga shares acquired: 269,095 shares Ownership in Psyga: 83.40% of share capital Private placement proceeds: $1,500,000 +5 more
8 metrics
Psyga shares acquired 269,095 shares Equity stake purchased in Psyga Bio at closing
Ownership in Psyga 83.40% of share capital Psyga Bio ownership on a fully diluted basis
Private placement proceeds $1,500,000 Cash wired to XTL treasury concurrent with acquisition closing
Initial consideration stake 33.36% of XTL capital ADSs issued to Psyga holders post‑issuance, pro‑rata basis
Milestone equity pool up to 25.02% of XTL capital Additional ADSs issuable upon three clinical/commercial milestones
ADS ratio 400 ordinary shares per ADS Each XTL ADS represents 400 ordinary shares
Clinical trials submitted 3 trials Trials planned with leading hospitals in Israel
Additional planned trials 4 trials Further studies targeted in the coming year

Previous Acquisition Reports

2 past events · Latest: Apr 29 (Positive)
Same Type Pattern 2 events
Date Event Sentiment 24h Move Catalyst
Apr 29 Psyga Bio acquisition Positive +54.8% Agreed all‑stock deal to acquire 100% of Psyga Bio with Psychedelic platform.
Jan 13 NeuroNOS acquisition Positive +56.7% Agreed to acquire 85% of NeuroNOS with autism and neuro‑oncology programs.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Acquisition announcements for XTLB have historically coincided with strong positive share‑price reactions.

Key Terms

gmp, active pharmaceutical ingredients, right to try, american depositary shares
4 terms
gmp regulatory
"operations will focus on an advanced clinical pipeline, a licensed GMP manufacturing facility"
Good Manufacturing Practice (GMP) is a set of regulatory standards and procedures that ensure products—especially medicines, medical devices, and related goods—are consistently made to meet safety, quality, and purity requirements. For investors, GMP compliance is like a factory’s hygiene and checklist system: it reduces the risk of product recalls, regulatory fines, and production stoppages, supports market access, and signals more reliable, lower-risk operations that can protect revenue and reputation.
active pharmaceutical ingredients technical
"formulation of psychedelic Active Pharmaceutical Ingredients (APIs) of medical grade"
The active pharmaceutical ingredient (API) is the specific chemical or biological substance in a medicine that produces the intended health effect — the ‘engine’ that treats, prevents or diagnoses a condition. Investors watch APIs because they determine a drug’s cost, quality, regulatory approval and patent protection; shortages, manufacturing problems or competition at the API level can directly affect a drug maker’s sales and valuation.
right to try regulatory
"opened fast-track access routes under the "Right to Try" law"
A legal pathway that allows seriously ill patients to try unapproved medicines or treatments outside of formal clinical trials when no approved options remain. For investors, it matters because wider access can alter demand, safety data, and public perception of a drug—similar to an emergency exit that lets more people use a product early but also raises the chances of unexpected outcomes that can affect a company’s regulatory path and reputation.
american depositary shares financial
"issuance of American Depositary Shares (ADSs) representing approximately 33.36% of XTL's capital"
American depositary shares (ADSs) are a way for investors in the United States to buy shares of foreign companies without dealing with international markets directly. They represent ownership in a foreign company's stock and are traded on U.S. stock exchanges, making it easier for American investors to buy, sell, and own parts of companies from around the world.

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

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expands its IP portfolio to clinical-stage biopharmaceutical assets

XTL Biopharmaceuticals (XTL) Completes the Acquisition of Psyga Bio and Establishes Psychedelic Biotechnology Platform

At a historic juncture and with unprecedented regulatory tailwinds in the US, XTL completes its strategic transformation and becomes a dedicated company in the field of global psychedelic medicine; operations will focus on an advanced clinical pipeline, a licensed GMP manufacturing facility, and a unique intellectual property (IP) library.

HERZLIYA, ISRAEL, June 30, 2026 (GLOBE NEWSWIRE) -- XTL Biopharmaceuticals Ltd. (NASDAQ and TASE: XTLB), is pleased to announce today the completion of the strategic acquisition of Psyga Bio Ltd. With the closing of the transaction, psychedelic operations become the exclusive core business of XTL, as part of the Company's strategy to lead the scientific intellectual property (IP) market.

XTL acquired 269,095 shares of Psyga Bio, representing approximately 83.40% of the issued and outstanding share capital of the company on a fully diluted basis. By doing so, XTL positions itself as one of the few public companies offering investors direct access to a complete scientific and industrial infrastructure  in the emerging field of psychedelic medicine.

The Strategic Assets and Competitive Advantages of XTL:

  • Advanced Clinical Pipeline Based on Psilocybin and its Derivatives: Psyga Bio is developing an advanced pipeline of products and formulations based on Psilocybin and its derivatives and additional psychedelic substances under strict regulatory licenses. These products are targeted for the treatment of severe mental health disorders, treatment-resistant depression, post-traumatic stress disorder (PTSD), anorexia, and addictions.
  • Independent Production Infrastructure (GMP-Ready Facility): The company holds a rare strategic asset in the industry, a licensed, pharmaceutical manufacturing facility for clinical trials, designated for the cultivation, extraction, isolation, and formulation of psychedelic Active Pharmaceutical Ingredients (APIs) of medical grade, ensuring operational independence and large-scale commercialization capabilities.
  • Exclusive Intellectual Property (IP) Library: A rich proprietary library of over 250 distinct and unique mushroom strains with high biological activity, providing the company with strong IP protection and perfect clinical product uniformity.
  • Global Scientific Leadership: The company's research and clinical activities are led in close partnership with Professor Dedi Meiri, one of the world's leading and most respected researchers in plant biology and natural-source drug development, which constitutes a scientific asset and a huge competitive advantage for the company.
  • Clinical Trials in Collaboration with Leading Hospitals in Israel: The company is in the process of submitting for the execution of three clinical trials with leading hospitals in Israel. In its roadmap are four additional clinical trials in the coming year. The company utilizes its existing infrastructure and IP to conduct several trials in parallel.

Concurrent with the completion of the acquisition, a cash amount of $1,500,000 was wired to the company's treasury as part of an approved private placement as further described in the Company’s filings with the Securities and Exchange Commission. This capital will be used directly to support and accelerate the clinical and business plans of the group.

Historic Regulatory Tailwind in the US: The FDA Accelerates Steps

We believe that the timing of the transaction's completion positions XTL in a perfect springboard position in the international market. In April 2026, US President Donald Trump signed a groundbreaking executive order instructing the FDA and DEA to dramatically accelerate (Fast-Track) the research, classification, and regulatory approvals of psychedelic drugs for the treatment of severe mental health disorders and post-traumatic stress disorder (PTSD).

The order specifically defined Ibogaine as a compound of supreme national importance for the treatment of discharged soldiers, allocated dedicated federal budgets, and opened fast-track access routes under the "Right to Try" law. Following this historic move, the FDA has already begun operating at an unprecedented speed to approve innovative clinical protocols. We believe that this shift in trend moves Psyga's field of activity into the heart of the mainstream medical establishment's consensus and has the potential to generate huge market potential for the company.

Details of the Financial Structure:

  • Stock-Based Consideration (Cash Preservation): The acquisition was completed through the issuance of American Depositary Shares (ADSs) representing approximately 33.36% of XTL's capital post-issuance (on a pro-rata basis). Each ADS represents 400 ordinary shares of the company.
  • Success-Based Milestone Mechanism (Milestones): In order to ensure complete alignment of interests with the shareholders, Psyga's shareholders will be entitled to receive an additional amount of up to 25.02% of XTL’s capital on the date of such issuance (approximately 8.34% for each milestone). These shares will be granted solely upon the achievement of three significant clinical and commercial milestones in the market.

The transaction was duly approved by the Audit Committee, the Board of Directors, and the general meeting of shareholders (including as an interested party transaction under the Israeli Companies Law).

Additionally, the company intends to file its financial statements for the year ending December 31, 2025, together with the annual Form 20-F, thereby maintaining transparency and full regulatory compliance before the markets in Israel and the US.

Cautionary Note Regarding Forward-Looking Statements

This communication contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. Any statements contained in this communication that are not statements of historical fact may be deemed forward-looking statements. Words such as “continue,” “will,” “may,” “could,” “should,” “expect,” “expected,” “plans,” “intend,” “anticipate,” “believe,” “estimate,” “predict,” “potential,” and similar expressions are intended to identify such forward-looking statements. All forward-looking statements involve significant risks and uncertainties that could cause actual results to differ materially from those expressed or implied in the forward-looking statements, many of which are generally outside the control of the Company and are difficult to predict. Examples of such risks and uncertainties include, but are not limited to, whether the Company will be able to successfully manage and integrate Psyga Bio.

Additional examples of such risks and uncertainties include, but are not limited to (i) the Company’s ability to successfully manage and integrate Psyga Bio and realize the milestones set out in the Purchase Agreement; (ii) the pending Nasdaq delisting determination and risk of delisting of the Company’s ADSs; (iii) clinical, regulatory and commercial risks relating to Psyga Bio’s pipeline, including Ibogaine-based products; (iv) unanticipated operating costs, transaction costs and actual or contingent liabilities; (v) the ability to attract and retain qualified employees and key personnel, including Professor Dedi Meiri; (vi) adverse effects of increased competition on the Company’s future business; (vii) the Company’s financing needs and ability to fund operations; (viii) the Company’s ability to protect its intellectual property; and (ix) local, industry and general business and economic conditions. Additional factors that could cause actual results to differ materially from those expressed or implied in the forward-looking statements can be found in the most recent annual report on Form 20-F and reports on Form 6-K filed by the Company with the Securities and Exchange Commission. The Company anticipates that subsequent events and developments may cause its plans, intentions and expectations to change. The Company assumes no obligation, and it specifically disclaims any intention or obligation, to update any forward-looking statements, whether as a result of new information, future events or otherwise, except as expressly required by law. Forward-looking statements speak only as of the date they are made and should not be relied upon as representing the Company’s plans and expectations as of any subsequent date.

For further information, please contact:

Investor Relations, XTL Biopharmaceuticals Ltd.

Email: info@xtlbio.com

www.xtlbio.com


FAQ

What did XTLB announce on June 30, 2026, regarding its acquisition of Psyga Bio?

XTL announced completion of acquiring about 83.40% of Psyga Bio, making psychedelic operations its exclusive core business. According to XTL, this positions the company as a public platform offering direct investor exposure to psychedelic clinical, manufacturing, and intellectual property infrastructure.

How does the Psyga Bio acquisition change XTLB’s business strategy?

The deal completes XTL’s transformation into a dedicated psychedelic medicine company, focused on psilocybin-based therapies and related substances. According to XTL, strategy now centers on clinical development, a licensed GMP facility, and leveraging its extensive mushroom-strain IP for mental health indications.

What is the financial structure and dilution impact of XTLB’s Psyga Bio acquisition?

XTL financed the deal through ADS issuance representing about 33.36% of its post-transaction capital, with up to 25.02% more upon milestones. According to XTL, this stock-based structure preserves cash while aligning Psyga shareholders’ rewards with future clinical and commercial achievements.

What clinical trials is XTLB planning after acquiring Psyga Bio?

XTL reports it is submitting three clinical trials with leading Israeli hospitals and planning four more within the coming year. According to XTL, programs target severe mental health disorders, treatment-resistant depression, PTSD, anorexia, and addictions, supported by its psychedelic infrastructure and IP.

What manufacturing and IP assets did XTLB gain through the Psyga Bio acquisition?

XTL gained a licensed, pharmaceutical manufacturing facility for clinical trials, covering cultivation and formulation of psychedelic APIs. According to XTL, it also acquired a proprietary library of over 250 highly active mushroom strains, intended to support consistent, IP-protected clinical products.

How could the 2026 US executive order on psychedelics affect XTLB’s Psyga platform?

XTL believes an April 2026 US executive order accelerating FDA and DEA psychedelic approvals creates a favorable regulatory backdrop. According to XTL, faster pathways and designated federal support may increase international market potential for Psyga’s psychedelic mental health treatments.

How will the $1,500,000 private placement support XTLB after the Psyga Bio deal?

A $1,500,000 cash amount was wired to XTL’s treasury alongside the acquisition as part of an approved private placement. According to XTL, these funds will directly support and accelerate the group’s clinical trials and broader business plans in psychedelic medicine.