Medicilon Delivers One Stop Preclinical Support as Yizhong Pharma Secures NMPA Clinical Approval for YXC‑001 Tri‑functional Antibody Fusion Protein and YXC‑002 4th‑Generation EGFR Kinase Inhibitor

On August 24, 2026 Yizhong Pharma, a STAR-Market-listed biotech company, reported it has obtained Clinical Trial Approval Notices from the National Medical Products Administration (NMPA) for two proprietary innovative drug candidates: YXC-001, a tri functional antibody fusion protein, and YXC-002, a 4th-generation EGFR kinase inhibitor.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

As Yizhong Pharma’s CRO partner, Medicilon executed full-scope preclinical studies (PD, PK, Tox) for YXC -001 under GLP requirements supporting China-US dual filings. For YXC-002, Medicilon completed full CMC deliverables (API, DP) alongside its complete preclinical package(PD, PK, Tox). High-quality datasets and on-time project delivery underpinned the successful IND approvals.

Scientific Progress: Two Novel Candidates Address Unmet Oncology Needs
Discovery landscape is advancing toward refined, differentiated and original innovation. Multi modal fusion antibodies and next-generation targeted small molecules represent key strategies to overcome clinical drug resistance and improve patient outcomes.

YXC-001 targets advanced solid tumors while YXC-002 is developed for non-small-cell lung cancer (NSCLC). Powered by novel mechanisms and compelling preclinical activity, both candidates may expand therapeutic options for difficult-to-treat patient populations.

YXC-001: First-in-Class Tri-functional Antibody Fusion Protein for Advanced Solid Tumors
YXC-001 is a first-in-class tri-functional antibody fusion protein designed to resolve the long standing efficacy toxicity trade off in advanced solid tumor therapy via structural engineering and tumor targeted delivery, representing a shift from single target blockade toward multi mechanism, spatially controlled immunomodulation.
The molecule integrates functional domains derived from a PD-1 antibody, anti-VEGF antibody and an optimized low-toxicity IL- 2 moiety. Engineered conformational changes to IL-2 eliminate systemic toxicity; antibody mediated targeting concentrates IL-2 within the tumor microenvironment for local activation.
This mechanism relieves immune suppression, remodels tumor vasculature to enhance T-cell infiltration, and expands intratumoral effector cells, amplifying anti tumor immunity while limiting systemic exposure-related risks. In mouse lung cancer models, YXC-001 demonstrated superior tumor growth inhibition compared with a PD-1 monoclonal antibody (Keytruda) and a PD-1/VEGF bispecific antibody at equivalent doses, with a clear dose response profile.
YXC- 002: 4th-Generation High Brain-Penetrant EGFR-TKI for NSCLC with Drug Resistance and CNS Metastases
YXC-002 in tablet formulation is Yizhong Pharma’s proprietary Class 1 small-molecule EGFR-TKI. It covers canonical and non-canonical EGFR driver and resistance mutations in NSCLC and is intended for patients with central nervous system (CNS) metastases.
Its unique structural design yields three core advantages
It confers activity against the C797S resistance mutation with high selectivity for mutant over wild type EGFR to minimize off target effects; it shows stronger anti tumor activity than BDTX 1535 (a Phase II stage 4th generation EGFR TKI), particularly against 19del sensitizing mutation and L858R T790M C797S triple mutation; and its molecular architecture enables robust blood brain barrier penetration.
The dual IND clearances mark a key transition from concept to clinical stage for Yizhong Pharma’s multifunctional antibody and small molecule targeted drug platforms, validating its original innovation capacity and differentiated pipeline strategy.
Medicilon’s One Stop Preclinical CRO Accelerates IND Progress
Medicilon deployed dedicated cross functional project teams for both programs, delivering end to end services covering CMC, PD, PK, Tox and regulatory support. Customized development strategies were implemented through close inter department collaboration.
The Medicilon’s pharmacodynamics team built bespoke in-vivo models for trispecific antibodies and EGFR- resistant tumors to match the projects’ cutting-edge requirements. Medicilon maintains a portfolio of more than 800 oncology pharmacology models, enabling comprehensive evaluation of small-molecule agents, monoclonal/bispecific antibodies, ADC/AOC modalities and CAR-T/CAR- NK cell therapeutics.

The Medicilon’s toxicology group tailored preclinical strategies according to each molecule’s structure and mechanism‑of‑action to generate robust safety data. The regulatory team provided full‑cycle support including dossier preparation, regulatory submission and CDE query responses, removing roadblocks throughout the IND review process.

Medicilon congratulates Yizhong Pharma on the clinical approval of YXC‑001 and YXC‑002. We look forward to positive clinical outcomes that will benefit patients. Moving forward, Medicilon will continue to enhance its integrated platform. With robust technical capabilities, reliable delivery and rigorous compliance frameworks, we will support more original‑innovation programs and accelerate the translation of novel drug concepts into clinical candidates.

(Press release, Shanghai Medicilon, AUG 24, 2026, View Source [SID1234670296])

Quest Diagnostics to Speak at the Morgan Stanley 24th Annual Global Healthcare Conference

On August 24, 2026 Quest Diagnostics Incorporated (NYSE: DGX), a leader in diagnostic information services, reported that Sam Samad, Executive Vice President & Chief Financial Officer, will speak on the company’s strategy, performance and the latest market developments and trends during the Morgan Stanley 24th Annual Global Healthcare Conference in New York City on Monday, September 14, 2026, at 10:00 a.m. Eastern Time.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

The fireside chat and Q&A session will be webcast live during the conference on the company’s investor relations page, which can be accessed at ir.QuestDiagnostics.com. In addition, the archived webcast will be available within 24 hours after the conclusion of the live event and will remain available until October 12, 2026.

(Press release, Quest Diagnostics, AUG 24, 2026, View Source [SID1234670295])

QIAGEN Appoints Jonathan M. Pratt as Chief Executive Officer

On August 24, 2026 QIAGEN N.V. (NYSE: QGEN; Frankfurt Prime Standard: QIA) reported that Jonathan M. Pratt has been appointed Chief Executive Officer, effective September 1, 2026. He brings to QIAGEN more than 25 years of international leadership experience across life sciences, laboratory technologies and healthcare.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

Jon Pratt most recently served as President and CEO of Filtration Group, leading the business through the completion of its sale to Parker-Hannifin Corporation in August 2026. He previously served as Senior Vice President of the Waters Division at Waters Corporation and as President of Beckman Coulter Life Sciences, a Danaher operating company, and held senior leadership positions at Pall Corporation.

Throughout his career, he has led global businesses spanning analytical instruments, laboratory technologies, software, consumables, services and bioprocessing applications. His experience includes commercial execution, portfolio management, operations and organizational development in markets closely aligned with QIAGEN’s portfolio and customer workflows.

The appointment follows a comprehensive search process. Jon Pratt was selected for his global industry knowledge, international leadership experience and proven track record of improving performance across global businesses. He will also be proposed for shareholder approval as a Managing Director at an Extraordinary General Meeting planned for the fourth quarter of 2026.

"The Supervisory Board unanimously concluded that Jon Pratt is the right leader for QIAGEN’s next phase," said Stephen H. Rusckowski, Chairman of the Supervisory Board of QIAGEN. "Jon combines deep knowledge of our markets with a strong international record of strengthening commercial execution and operational performance. His experience across life sciences and laboratory technologies is directly relevant to QIAGEN’s portfolio and customers. Building on our strong foundation, we are confident he will advance our commitment to solid profitable growth. On behalf of the Supervisory Board, I also want to thank Thierry Bernard for his leadership, his many contributions to QIAGEN and his support in ensuring continuity during this transition."

"QIAGEN is an iconic and trusted brand in life sciences and molecular diagnostics, built on scientific rigor, quality and technologies that support critical laboratory workflows worldwide," Jon Pratt said. "What attracted me to QIAGEN is the combination of talented teams, a differentiated portfolio and close customer relationships. My first priority will be to listen to QIAGEN teams and customers, learn more about the business and understand where we can sharpen our choices, strengthen execution and create greater impact. I look forward to working with the team to advance our vision of making improvements in life possible."

Thierry Bernard will step down as CEO and Managing Director and will support an orderly transition through the end of the year.

QIAGEN has reaffirmed its outlook for the third quarter and full-year 2026. QIAGEN remains focused on delivering solid profitable growth by advancing its growth pillars, improving operating efficiency and allocating capital to the highest-return opportunities.

As previously communicated, the Supervisory Board continues to evaluate opportunities, with independent financial and legal advisors, as part of its strategic review to create value for shareholders and other stakeholders relative to QIAGEN’s standalone business plan and long-term strategic objectives.

About Jonathan M. Pratt

Jon Pratt is an experienced global executive with more than 25 years of leadership experience across life sciences, laboratory technologies and healthcare. Before joining QIAGEN, he served as President and Chief Executive Officer of Filtration Group, a global filtration and separation science company, where he led the business through continued growth and the completion of its sale to Parker-Hannifin Corporation in August 2026. He previously served as Senior Vice President of the Waters Division at Waters Corporation and as President of Beckman Coulter Life Sciences, a Danaher operating company, and held senior leadership positions at Pall Corporation. He holds a Bachelor of Science in chemistry from the University of Reading in the United Kingdom and an MBA from New York University Stern School of Business.

(Press release, Qiagen, AUG 24, 2026, View Source;Pratt-as-Chief-Executive-Officer/default.aspx [SID1234670294])

Jemperli (dostarlimab) accepted for priority review by the US FDA for dMMR/MSI-H locally advanced rectal cancer

On August 24, 2026 GSK plc (LSE/NYSE: GSK) reported the US Food and Drug Administration (FDA) has accepted for priority review a supplemental Biologics License Application (sBLA) for Jemperli (dostarlimab) for patients with previously untreated stage II and III mismatch repair deficient (dMMR)/microsatellite instability-high (MSI-H) locally advanced rectal cancer. The FDA has assigned a PDUFA action date of February 2027. The application is also eligible for expedited review through the National Priority Voucher program, which could result in an earlier FDA decision1.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

Rectal cancer, a type of bowel cancer, affects around 770,000 people globally each year2 and approximately 5-10% of cases have the dMMR/MSI-H subtype3. Chemotherapy, radiation and surgery are the standard of care and while often effective, they can have lasting adverse effects on bowel, urinary and sexual function, fertility and overall quality of life4,5,6.

The application is based on positive data from the registrational phase II, single-arm AZUR-1 trial, which met its primary objective by demonstrating a meaningful and sustained clinical complete response rate for 12 months (cCR12) with no detectable signs of cancer for at least one year. In interim data, the safety and tolerability profile of dostarlimab was generally consistent with its well-characterised and manageable safety profile observed across solid tumours. These data will be submitted for presentation at a scientific congress later in 2026.

AZUR-1 results represent a substantial improvement compared to the historical standard of care7. The data support the potential for dostarlimab, if approved, to become the first immunotherapy capable of eliminating or delaying the need for chemotherapy, radiation and surgery for some patients in this population. These findings build on earlier research conducted with Memorial Sloan Kettering Cancer Center (MSK), which first demonstrated the potential for dostarlimab to achieve clinical complete responses without other treatments in patients with dMMR/MSI-H locally advanced rectal cancer.

Dostarlimab was previously granted Fast Track and Breakthrough Therapy Designations in this setting8,9. The application has also been accepted under Project Orbis, an FDA Oncology Center of Excellence initiative that enables coordinated reviews by international health authorities and may support earlier regulatory decisions and patient access. Regulatory decisions remain independent in each country.

About stage II and III dMMR/MSI-H locally advanced rectal cancer
Rectal cancer affects around 770,000 people globally each year2. Around 5–10% of rectal cancers are mismatch repair-deficient (dMMR) or microsatellite instability-high (MSI-H)3. These tumours have a specific genetic characteristic where they are unable to properly repair DNA damage, leading to an accumulation of mutations. This unique biological feature often makes them highly responsive to immunotherapies like dostarlimab10,11. These biomarkers are most commonly found in endometrial, colorectal and other gastrointestinal cancers, but can also be present in other solid tumours12.

About AZUR-1
AZUR-1 is a global, open-label, single-arm, registrational phase II trial evaluating dostarlimab monotherapy in patients (n=154) with previously untreated stage II and III dMMR/MSI-H locally advanced rectal cancer. The trial was designed to assess sustained clinical complete responses for 12 months (cCR12) and determine whether dostarlimab alone could enable patients to avoid chemotherapy, radiation and surgery. Patients received nine cycles of dostarlimab over six months, administered as a 500mg intravenous infusion every three weeks. In interim data, the safety and tolerability profile of dostarlimab was generally consistent with its well-characterised and manageable safety profile observed across solid tumours.

The AZUR-1 results represent a substantial improvement compared to the historical standard of care. They build on earlier research conducted in collaboration with Memorial Sloan Kettering Cancer Center, which first demonstrated the potential for dostarlimab to achieve clinical complete responses without other treatments in patients with dMMR/MSI-H locally advanced rectal cancer.

About Jemperli  
Jemperli, a programmed death receptor-1 (PD-1)-blocking antibody, is the backbone of GSK’s ongoing immuno-oncology based research and development programme. A robust clinical trial programme includes studies of Jemperli alone and in combination with other therapies in gynaecologic, colorectal and head and neck cancers, as well as where there are opportunities for transformational outcomes.

Jemperli was discovered by AnaptysBio, Inc. and licensed to TESARO, Inc., under a collaboration and exclusive license agreement signed in March 2014. Under this agreement, GSK is responsible for the ongoing research, development, commercialisation and manufacturing of Jemperli.

More information about the product and its indications is available at EU product information13 and US product information14.  Jemperli is not currently approved anywhere in the world for locally advanced rectal cancer.

(Press release, GlaxoSmithKline, AUG 24, 2026, View Source [SID1234670293])

Valerio Therapeutics announces signing of definitive agreements for the acquisition of Etherna Immunotherapies, building a leading platform in targeted RNA, and €40.25 million PIPE financing from new and existing investors

On August 24, 2026 Valerio Therapeutics (FR0010095596 – ALVIO), a biotechnology company pioneering next-generation precision-guided RNA therapeutics ("Valerio" or the "Company"), reported the signing of a definitive share purchase agreement (the "SPA") and of the related contribution agreement (the "Contribution Agreement") for the acquisition of 100% of the share capital and voting rights of Etherna Immunotherapies NV ("Etherna") (the "Acquisition"), based on an enterprise value of €30 million, and a €40.25 million private investment in public equity (PIPE) financing supported by existing shareholders and new investors (the "Financing").

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

"The acquisition of Etherna marks a decisive step in Valerio’s strategy: to build a leading player in RNA therapeutics. By combining Etherna’s RNA and LNP platforms with our proprietary cell-targeting technologies, we are creating a powerful innovation engine designed to accelerate the development of next-generation RNA medicines. Most importantly, our combined platforms enable us to overcome a bottleneck that has held the field back for decades: reaching tissues beyond the liver and, in doing so, opening the way to the treatment of a broad range of diseases that have so far been beyond the reach of conventional mRNA delivery." said Gilles Besin, Ph.D., CEO of Valerio.

"Signing this agreement is a defining moment for Etherna, and I could not be prouder of what our team has built with the support of our investors. Over the past years, we have turned a decade of mRNA and LNP expertise into platforms capable of reaching far beyond what conventional mRNA and delivery and manufacturing technologies could ever achieve. Joining forces with Valerio gives that platform the scale, the targeting capabilities and the resources to move faster and further than we could alone. I want to thank our shareholders, partners and, above all, our people for their trust and dedication in getting us here. Together with Valerio, Etherna’s science and manufacturing will deliver transformative medicines to patients who need them most.", said Bernard Sagaert, CEO of Etherna.

Terms and Conditions of the Acquisition

The Acquisition marks a major milestone in Valerio’s strategy to build a leading platform in targeted nucleic acid medicines. By uniting three complementary technology platforms – nucleic acid chemistry, LNP delivery and targeted moiety engineering – within a fully integrated biotech supported by in-house manufacturing capabilities, the Acquisition aims to position Valerio to accelerate the development of next-generation RNA medicines targeting tissues beyond the liver.

The Acquisition will be settled through (i) a cash consideration, fully funded by the Financing, and (ii) a share consideration through contributions in kind of Etherna shares (the "Contributions") to the Company.

The Contributions remain subject to Valerio shareholders approval at an extraordinary general meeting to be convened for that purpose expected to be held on or about October 6, 2026. Approval is secured by irrevocable voting undertakings from existing shareholders representing more than 70% of the voting rights of the Company.

Shares issued as consideration for the Contributions will be valued at the same Subscription Price as the New Shares issued in the Financing. A contribution auditor (commissaires aux apports) has been appointed to assess the valuation of the Contributions and issue a fairness report. Certain lenders and managers of Etherna will also subscribe to new Valerio shares through the set-off of their receivables owed by Etherna at the same subscription price.

The consideration for the Acquisition is based on an enterprise value of €30 million (on a debt-free, cash-free basis) subject to customary purchase price adjustments and contingent earn-out payments.

Main Terms of the Financing

The Financing was carried out through the issuance of 68,220,333 new ordinary shares (the "New Shares"), at a subscription price of €0.59 per share (i.e., a par value of €0.01 and an issuance premium of €0.58 per New Share) (the "Subscription Price"), representing a discount of 25% to the 3-day VWAP prior to pricing.

The New Shares are issued through a capital increase without shareholders’ preferential subscription rights by way of an offering referred to in paragraph 1 of article L. 411-2 of the French Monetary and Financial Code (Code monétaire et financier), and pursuant to the decisions of the Company’s Chief Executive Officer on August 21, 2026, acting upon sub-delegation of the Company’s Board of Directors on July 30, 2026, in accordance with the delegations granted pursuant to the 15th resolutions and within the limits set by the 22nd resolution of the Company’s combined shareholders’ meeting held on June 16, 2026 (the "General Meeting").

The issuance of the 68,220,333 New Shares will result in a capital increase of €40.25 million (i.e., a nominal amount of €682,203.33 and a total issuance premium of €39,567,793.14), representing approximately 13.7% of the Company’s share capital and voting rights outstanding before the Financing.

Existing shareholders Artal International SCA, Financière de la Montagne and Saint James Luxembourg subscribed for €18.0 million, €7.0 million and €1.0 million respectively. Artal International SCA and Financière de la Montagne, who are also members of or represented on Valerio’s Board of Directors, did not take participate in the vote on the Financing at the Board of Directors’ meeting held on July 30, 2026.

Following the settlement-delivery of the New Shares expected on August 26, 2026, the Company’s share capital will be €5,676,686.34 divided into 567,668,634 ordinary shares.

Impact of the Financing on Cash Flow and Use of Proceeds

The Company intends to use the net proceeds from the Financing, together with its existing cash and cash equivalents, to: (i) fund the cash component of the consideration payable in connection with the Acquisition; (ii) advance its proprietary pipeline, including VTX-001, VTX-002 and VTX-003, as well as IND-enabling activities for VTX-001; (iii) integrate Etherna into Valerio, including by investing in and scaling Etherna’s GMP manufacturing capabilities at its Niel facility to support the Company’s clinical supply requirements and build internal capacity for mRNA and LNP production, and by combining the two organizations’ research, technical operations and quality functions on a single platform; and (iv) fund working capital and other general corporate purposes.

The expected use of net proceeds reflects the Company’s current intentions, based on its present plans and business condition. The amounts and timing of the Company’s actual expenditures will depend on numerous factors, including the progress of its development programs, the timing and outcome of the integration of Etherna, and any unforeseen cash needs.

Based on its current operating plan and forecasted expenses, and taking into account its cash and cash equivalents together with the net proceeds from the Financing, the Company believes it has sufficient resources to fund its planned operating expenses and capital expenditure requirements for at least 18 months following the closing of the Financing. This estimate is based on assumptions that may prove to be incorrect, and the Company may use its capital resources sooner than currently expected.

Shareholding Structure after the Financing

On an illustrative basis, a shareholder holding 1% of the Company’s share capital before the Financing and who did not participate in the Financing will hold 0.88% of the Company’s share capital after the issuance of the New Shares.

To the Company’s knowledge, the shareholding structure, on a non-diluted basis, before and after the Financing, breaks down as follows:

Before Financing After Financing
Shareholders Number of Shares % Share Capital % Voting Rights Number of Shares % Share Capital % Voting Rights
Artal International SCA 219 981 537 44.04 % 44.04 % 250 490 011 44.1% 44.1%
Financière de la Montagne 90 486 732 18.12 % 18.12 % 102 351 138 18.0% 18.0%
Fidat Ventures 43 478 260 8.71 % 8.71 % 43 478 260 7.7% 7.7%
SCP Esperanza 2019 41 977 806 8.40 % 8.40 % 41 977 806 7.4% 7.4%
Others 103 523 966 20.73 % 20.73 % 129 371 419 22.8% 22.8%
499 448 301 100.00 % 100.00 % 567 668 634 100.00 % 100.00 %
Lock-up Agreements

In connection with the Financing, the Company has entered into a lock-up agreement restricting the issuance of additional ordinary shares for a period ending ninety (90) calendar days following the date of settlement-delivery, subject to customary exceptions.

In addition, the investors subscribing to the Financing, have agreed to a sixty (60) calendar days lock-up on the New Shares, following the date of settlement-delivery, subject to customary exceptions.

Settlement-delivery of the Financing

The admission of the New Shares to trading on the Euronext Growth market in Paris is scheduled for the time of settlement and delivery, which is expected to take place on August 26, 2026.

The New Shares will be immediately assimilated to the Company’s existing shares already traded on Euronext Growth in Paris, and will be able to be traded, from their issuance, on the same listing line (ISIN code: FR0010095596).

The Financing has not given rise to a prospectus submitted for approval by the AMF, nor to an information document containing the information set out in Annex IX of Regulation (EU) 2017/1129, as amended.

Risk Factors

The Company draws the public’s attention to the risk factors related to the Company and its activities presented in the 2025 annual financial report published on April 28, 2026, which is available free of charge on the website of the Company (View Source).

In addition, investors are invited to consider the following risks: (i) shareholders’ stake in the Company will be diluted further to the issuance of the New Shares for the shareholders who did not participate in the Financing, (ii) the market price for the Company’s shares may fluctuate and fall below the subscription price of the shares issued pursuant to the Financing, (iii) the volatility and liquidity of the Company’s shares may fluctuate significantly, (iv) sales of the Company’s shares may occur on the market and have a negative impact on the market price of the shares, and (v) the Company’s shareholders could undergo a potentially material dilution resulting from any future capital increases that are needed to finance the Company.

Advisors

Van Lanschot Kempen NV is acting as exclusive financial advisor for the Acquisition and as Sole Placement Agent in connection with the Financing. Goodwin Procter LLP is acting as legal counsel to Valerio Therapeutics.

Moelis & Company is acting as financial advisor to Etherna. Deloitte (Belgium) and August Debouzy (France) are acting as legal counsels to Etherna.

(Press release, eTheRNA, AUG 24, 2026, View Source [SID1234670292])