OPM Announces Its 2025 Annual Results and Provides an Update on Its Clinical Developments

On April 30, 2026 Oncodesign Precision Medicine (OPM) (ISIN: FR001400CM63; Ticker symbol: ALOPM), a biopharmaceutical company specializing in precision medicine for the treatment of resistant and metastatic cancers, reported its 2025 financial results, as approved by the Board of Directors on April 27, 2026.

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Philippe Genne, co-founder, President and Chief Executive Officer of OPM said: "2025 is a pivotal year for OPM, marked by the maturation of our clinical assets—particularly OPM-101 and OPM-201—and by a strong refocusing of our investments on our priority programs. OPM-101 continues its development in immuno-oncology with the approval to initiate the REVERT study, while OPM-201 confirms its strategic potential in Parkinson’s disease with the support of the Michael J. Fox Foundation. These advances reinforce the positioning of our programs as mature and attractive assets for industrial partners. In an environment where funding remains constrained, we are simultaneously maintaining rigorous management of our resources to secure our trajectory and maximize the value of our assets."

Karine LIGNEL, Deputy CEO and COO of Oncodesign Precision Medicine, adds: "In 2025, we strengthened our operational discipline and focused our efforts on the programs with the greatest potential to create value. The scientific progress made on OPM-101 and OPM-201 confirms the validity of our strategy, despite a funding environment that remains challenging for publicly traded biotechnology companies."

Oncodesign Precision Medicine – Income Statement

in M€

Audited data

2025

2024

Evolution

in %

in value

Revenues

0.26

0.21

+26%

0.26

Other revenues and operating income

1.55

1.43

+9%

1.55

Total revenues and operating income

1.81

1.64

+11%

0.18

Change in inventory

13.00

NS

13.00

Purchases consumed

(3.53

)

(6.51

)

-46%

2.98

Personnel costs

(2.59

)

(2.59

)

+0%

(0.00

)

Other operating expenses

(0.05

)

(0.01

)

+492%

(0.04

)

Taxes and duties

(0.06

)

(0.07

)

-21%

0.02

Net change in depreciation and amortization

(2.88

)

(0.26

)

+1013%

(2.62

)

Total operating expenses

3.89

(9.44

)

na

13.34

Operating result

5.71

(7.81

)

na

13.51

Financial expenses and income

(0.19

)

(0.15

)

+26%

0.04

Non-recurring expenses and income

Income tax

Net result

5.48

(7.21

)

na

12.69

Overview of Our Development Programs and Technologies in 2025

In 2025, OPM continued to advance its priority assets, particularly OPM-101 in oncology and OPM-201 for the treatment of Parkinson’s disease, accelerating the transition to advanced clinical phases.

OPM-101 confirmed a favorable safety and activity profile in Phase 1 and received approval to initiate the REVERT study (Phase 1b/2a) in immuno-oncology, in combination with pembrolizumab.

Meanwhile, OPM-201 has achieved key milestones with the consolidation of its data, the validation of its mechanism of action, and the signing of a strategic partnership with the Michael J. Fox Foundation, which materialized in early 2026 with significant funding (~$7 million) to prepare for its entry into clinical trials for Parkinson’s disease.

This momentum has been accompanied by a significant improvement in operational performance. Operating revenue rose to €1.81 million (+11%), consisting mainly of government grants and reversals of provisions.

A significant effort to control costs was made in 2025, particularly regarding consumable purchases (-46%), reflecting a refocus on priority programs and an optimization of subcontracting expenses. Personnel expenses remained stable, while other operating expenses remained limited.

Operating income amounted to €5.71 million, compared to a loss of €7.81 million in 2024. This change includes a one-time effect related to the recognition of a positive inventory change of €13 million, corresponding to the consolidation of OPM-201 active ingredient inventories.

Oncodesign Precision Medicine – R&D expenditure

in M€

Analytical data

2025

2024

Evolution

In %

in value

Partnerships

0.8

1.8

– 55%

– 1.0

Licensing

2.3

4.8

– 51%

– 2.5

Total R&D expenses

3.13

6.58

– 52%

– 3.45

R&D investments declined in 2025 due to refocusing on priority programs, notably OPM-101, and a reduction in external spending on partnership and non-strategic programs.

OPM received €0.53 million in Research Tax Credits in 2025, down from 2024, due to lower R&D spending and changes in applicable tax rules.

Cash position of €2.1 million as of December 31, 2025

OPM’s cash position stood at €2.11 million as of December 31, 2025, compared to €5.27 million at the start of the fiscal year, reflecting cash outflows related to the funding of R&D activities and strategic programs during the period.

At the same time, the Company has strengthened its financing and financial flexibility, notably through convertible bonds (ORA) and government programs, while implementing a cost optimization plan that generated €5.9 million in savings during fiscal year 2025.

OPM is also continuing discussions with industrial and financial partners to secure the next stages of development.

The Company has also secured a 12-month extension of its bank loan maturity to preserve its financial flexibility. The Company’s ability to continue as a going concern beyond December 31, 2026, remains contingent upon securing additional financing, implementing further cost reductions, or entering strategic partnerships, none of which had been finalized as of the balance sheet date.

Outlook for 2026

In 2026, OPM will continue preparations for the Phase 1b trial of OPM-201 with funding from the Michael J. Fox Foundation, while continuing to seek industrial or financial partners to secure the next clinical stages.

In addition, the Phase 1b/2a trial of OPM-101 is expected to begin before the end of 2026, with the study expected to conclude by the end of 2028. Similarly, a search for partners is underway for this compound.

Finally, the other programs will progress according to the opportunities presented by the funding OPM may receive throughout the year.

Availability of the 2025 Annual Financial Report

The 2025 Annual Financial Report will be available on the company’s website on April 30, 2026.

(Press release, Oncodesign Precision Medicine, APR 30, 2026, View Source [SID1234664987])

QUARTERLY ACTIVITIES & APPENDIX 4C CASH REPORT

On April 30, 2026 Imugene reported quarterly report ended March 2026.

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(Press release, Imugene, APR 30, 2026, View Source [SID1234669282])

Labcorp Announces 2026 First Quarter Results; Raises Full Year 2026 Guidance

On April 30, 2026 Labcorp Holdings Inc (NYSE: LH), a global leader of innovative and comprehensive laboratory services, reported results for the first quarter ended March 31, 2026 and updated full-year guidance.

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"Labcorp delivered another quarter of strong results, with robust growth and double-digit Adjusted EPS growth driven by continued momentum across our Diagnostics and Central Laboratory businesses," said Adam Schechter, Chairman and CEO of Labcorp. "Health systems, providers, consumers, and biopharmaceutical customers are increasingly turning to Labcorp as their partner of choice for their complex, innovative testing needs. Our investments in advanced technologies, including robotics and AI, are improving the customer experience and transforming the way we operate. Driven by continued progress across our strategic priorities, we are raising our full year Adjusted EPS guidance to $18.03 at the midpoint of the range, an increase of $0.13."

Labcorp continues to advance its strategic priorities:

Be a partner of choice for health systems and regional and local laboratories:

Announced a nationwide strategic collaboration with Children’s Hospital of Philadelphia (CHOP) to expand access to cutting-edge diagnostics for pediatric patients.
Completed the acquisition of select assets of Crouse Health’s Laboratory Alliance of Central New York and executed an agreement with Crouse Health to manage their inpatient labs.
Lead in specialty testing:

Announced a collaboration with Illumina to expand access to advanced genomic testing in oncology to deliver more precise biomarker insights.
Expanded nationwide access to the first FDA-approved companion diagnostic that helps identify patients with platinum‑resistant ovarian cancer who may benefit from Merck’s KEYTRUDA and KEYTRUDA QLEX.
Launched the Labcorp Fentanyl Visual Urine Test, an FDA‑cleared rapid screening test that delivers results in just 10 minutes and assesses possible fentanyl exposure for up to 48 hours.
Shape our future through technology and innovation:

Launched an AI-powered, real-world data platform with Amazon Web Services (AWS) and Datavant to accelerate Alzheimer’s research.
Expanded a collaboration with PathAI to deploy AISight Dx, an FDA-cleared digital pathology platform.
Announced a collaboration with Optum.ai to apply AI capabilities to streamline laboratory operations, improve efficiency, and enhance the patient and provider experience.
Drive personalized health solutions:

Grew Consumer Health and expanded the Labcorp OnDemand test portfolio with new tests for insulin resistance and pancreatic function, as well as customizable men’s and women’s health tests.
In May, the company will launch MyLabcorp, a secure, AI-powered mobile app that brings an individual’s test results and health data together with clinical guidance to help consumers better understand their test results.
Labcorp also remains committed to a disciplined allocation of capital. In the first quarter of 2026, the company invested $202.2 million in acquisitions, repurchased $98.0 million of stock, and paid out $61.2 million in dividends. On April 9, 2026, the company announced a quarterly cash dividend of $0.72 per share of common stock, payable on June 11, 2026, to stockholders of record at the close of business on May 29, 2026.

(Press release, LabCorp, APR 30, 2026, View Source [SID1234664970])

Guardant Health Announces Multi-Year Strategic Collaboration with Nuvalent to Develop Companion Diagnostics and Support Potential Commercialization of Targeted Cancer Therapies Using the Guardant Infinity™ Platform

On April 30, 2026 Guardant Health, Inc. (Nasdaq: GH), a leading precision oncology company, reported a multi-year strategic collaboration with Nuvalent, Inc. (Nasdaq: NUVL), a clinical-stage biopharmaceutical company focused on creating precisely targeted therapies for clinically proven kinase targets in cancer, to support the development and potential commercialization of Nuvalent’s oncology pipeline using the tissue and liquid offerings of the Guardant Infinity platform.

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The collaboration reflects the growing importance of precision diagnostics in oncology drug development, where biomarker-driven approaches are increasingly essential for identifying appropriate patient populations, improving trial efficiency, and supporting regulatory approvals.

As key components of the collaboration, Guardant Health and Nuvalent plan to:

Utilize Guardant’s portfolio of tissue and liquid biopsy tests to support certain Nuvalent global clinical studies;
Evaluate opportunities to develop Guardant tissue and/or liquid biopsy assays as companion diagnostics (CDx) to support potential regulatory approvals of Nuvalent’s current investigational candidates; and,
Collaborate on the global commercialization of Nuvalent’s product candidates, if approved, and Guardant companion diagnostics across major global key markets.

(Press release, Guardant Health, APR 30, 2026, View Source [SID1234664988])

Pinetree Therapeutics Announces Exercise of Option to License EGFR Degrader Program by AstraZeneca

On April 29, 2026 Pinetree Therapeutics, Inc. ("Pinetree"), a biotechnology company pioneering next-generation targeted protein degradation approaches for cancer and other serious diseases, reported that AstraZeneca (LSE/STO/NYSE: AZN) has exercised its option under the companies’ previously announced agreement to obtain an exclusive global license to develop and commercialize PTX-299, a first-in-class bispecific antibody degrader targeting EGFR.

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The option exercise follows encouraging preclinical progress and represents an important milestone in the collaboration between the two companies. Under the terms of the agreement, AstraZeneca will assume responsibility for global development and commercialization of the therapeutic candidate.

"This milestone marks an important validation of our AbReptor platform," said Hojuhn Song, Ph.D., Founder and CEO of Pinetree Therapeutics. "We are pleased that AstraZeneca has exercised its option to advance PTX-299, and we look forward to seeing them continue the development of this promising therapeutic candidate. By combining Pinetree’s breakthrough protein degradation platform with AstraZeneca’s global expertise in cancer drug development, we believe that PTX-299 has the potential to bring a meaningful new treatment option to patients with EGFR-driven cancers."

EGFR plays a critical role in the growth and survival of cells in multiple tumor types. While EGFR-targeted therapies have transformed patient outcomes, resistance can develop, highlighting the need for new therapeutic strategies. By leveraging Pinetree’s antibody-based protein degradation technology, PTX-299 is designed to selectively eliminate disease-driving EGFR proteins rather than simply inhibiting their activity, potentially overcoming key resistance mechanisms.

The therapeutic candidate was developed using AbReptor, Pinetree’s proprietary multispecific antibody-based targeted protein degradation platform. In contrast to conventional monoclonal antibodies that rely on functional inhibition, AbReptor drives the active removal of disease-associated proteins through targeted degradation. By enabling the elimination of membrane-bound and extracellular targets, this platform extends beyond the limitations of traditional inhibition-based antibody therapies.

Under the terms of the agreement, AstraZeneca’s exercise of the option triggers a $25 million option closing payment to Pinetree. Pinetree is also eligible to receive potential future development, regulatory, and commercial milestone payments and tiered royalties on global net sales if the product is successfully developed and commercialized. The total potential value of the agreement exceeds $500 million.

(Press release, PineTree Therapeutics, APR 29, 2026, View Source [SID1234664909])