Test 2 Headline 30.01.26

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ABOUT SANDOZ
Sandoz (SIX: SDZ; OTCQX: SDZNY) is the global leader in affordable medicines, with a growth strategy driven by its Purpose: pioneering access for patients. More than 20,000 people of 100 nationalities work together to ensure 900 million patient treatments are provided by Sandoz, generating substantial global healthcare savings and an even larger social impact. Its leading portfolio of approximately 1,300 products addresses diseases from the common cold to cancer. Headquartered in Basel, Switzerland, Sandoz traces its heritage back to 1886. Its history of breakthroughs includes Calcium Sandoz in 1929, the world’s first oral penicillin in 1951, and the world’s first biosimilar in 2006. In 2024, Sandoz recorded net sales of USD 10.4 billion.

Heidelberg Pharma Received Development Milestone Payment from Partner Takeda

Heidelberg Pharma AG

/ Key word(s): Miscellaneous

Heidelberg Pharma Received Development Milestone Payment from Partner Takeda

29.01.2026 / 13:27 CET/CEST

The issuer is solely responsible for the content of this announcement.


PRESS RELEASE

Heidelberg Pharma Received Development Milestone Payment from Partner Takeda

Ladenburg, Germany, 29 January 2026 – Heidelberg Pharma AG (FSE: HPHA), a clinical stage biotech company developing innovative Antibody Drug Conjugates (ADCs), today announced that it has received a milestone payment under the terms of its license agreement with partner Takeda based on the achievement of a clinical development milestone for Takeda’s investigational medicine that utilizes Amanitin-based Antibody Drug Conjugate (ATAC) technology licensed from Heidelberg Pharma. With the dosing of the first patient in a Phase I/II clinical trial in patients with solid tumors, a milestone payment to Heidelberg Pharma became due. Financial details were not disclosed.

Dr. Dongzhou Jeffery Liu, Chief Executive Officer of Heidelberg Pharma AG, commented: “We are very delighted that our partner Takeda is progressing the development of their investigational medicine that utilizes ATAC technology, and that we have received the according milestone payment. We congratulate the Takeda team and wish them every success in clinical development. With this, three candidates that leverage ATAC technology are now in clinical development, two that are proprietary to Heidelberg Pharma including HDP-101 (INN: pamlectabart tismanitin) and HDP-102, and one under the responsibility of our partner. For us, this is a further validation of the potential of our unique Amanitin-based ADC technology.”

Takeda exclusively licensed the worldwide development and commercialization rights from Heidelberg Pharma for the use of the ATAC technology with an antibody directed to a defined target and the resulting product candidate. Under the terms of the agreement, Takeda is responsible for the development, as well as commercialization, of the resulting product candidate.

About Heidelberg Pharma

Heidelberg Pharma is a biopharmaceutical company working on a new treatment approach in oncology and developing novel drugs based on its ADC technologies for the targeted and highly effective treatment of cancer. ADCs are antibody-drug conjugates that combine the specificity of antibodies with the efficacy of toxins to fight cancer. Selected antibodies are loaded with cytotoxic compounds, that are transported into diseased cells. Inside the cells, the toxins then unleash their effect and kill the diseased cells.

Heidelberg Pharma is the first company to use the compound Amanitin from the green death cap mushroom in cancer therapy. The biological mechanism of action of the toxin represents a new therapeutic modality and is used as a compound in the Amanitin-based ADC technology, the so-called ATAC technology.

The lead candidate HDP-101 (INN: pamlectabart tismanitin) is a BCMA ATAC in clinical development for multiple myeloma. The candidate has been granted Orphan Drug Designation and Fast Track Designation from the FDA. A second ATAC candidate, HDP-102 is in clinical development stage in Non-Hodgkin Lymphoma. HDP-103 against metastatic castration-resistant prostate cancer and HDP-104 targeting gastrointestinal tumors such as colorectal cancer have completed preclinical development. Heidelberg Pharma is open for partnering.

The company is based in Ladenburg, Germany, and is listed on the Frankfurt Stock Exchange: ISIN DE000A11QVV0 / WKN A11QVV / Symbol HPHA. More information is available at www.heidelberg-pharma.com

ATAC® is a registered trademark of Heidelberg Pharma Research GmbH. 

Contact
Heidelberg Pharma AG
Sylvia Wimmer
Director Corporate Communications
Tel.: +49 89 41 31 38-29
E-Mail: investors@hdpharma.com
Gregor-Mendel-Str. 22, 68526 Ladenburg
 
IR/PR-Support
MC Services AG
Katja Arnold (CIRO)
Managing Director & Partner
Tel.: +49 89 210 228-40
E-Mail: katja.arnold@mc-services.eu
 

This communication contains certain forward-looking statements relating to the Company’s business, which can be identified by the use of forward-looking terminology such as “estimates”, “believes”, “expects”, “may”, “will”, “should”, “future”, “potential” or similar expressions or by a general discussion of the Company’s strategy, plans or intentions. Such forward-looking statements involve known and unknown risks, uncertainties and other factors, which may cause our actual results of operations, financial condition, performance, achievements, or industry results, to be materially different from any future results, performance or achievements expressed or implied by such forward-looking statements. Given these uncertainties, prospective investors and partners are cautioned not to place undue reliance on such forward-looking statements. We disclaim any obligation to update any such forward-looking statements to reflect future events or developments.


29.01.2026 CET/CEST Dissemination of a Corporate News, transmitted by EQS News – a service of EQS Group.
The issuer is solely responsible for the content of this announcement.

The EQS Distribution Services include Regulatory Announcements, Financial/Corporate News and Press Releases.


Language: English
Company: Heidelberg Pharma AG
Gregor-Mendel-Str. 22
68526 Ladenburg
Germany
Phone: +49 (0)89 41 31 38 – 0
Fax: +49 (0)89 41 31 38 – 99
E-mail: investors@hdpharma.com
Internet: www.heidelberg-pharma.com
ISIN: DE000A11QVV0
WKN: A11QVV
Listed: Regulated Market in Frankfurt (Prime Standard); Regulated Unofficial Market in Dusseldorf, Munich, Stuttgart, Tradegate BSX
EQS News ID: 2268116

 
End of News EQS News Service

2268116  29.01.2026 CET/CEST

Eckert & Ziegler on Track as Planned and Achieves Another Record Year in 2025

Eckert & Ziegler SE

/ Key word(s): Preliminary Results

Eckert & Ziegler on Track as Planned and Achieves Another Record Year in 2025

29.01.2026 / 12:20 CET/CEST

The issuer is solely responsible for the content of this announcement.


Fiscal Year 2025 (preliminary):

  • Sales: approx. € 312 million (PY: € 295.8 million)
  • EBIT before special items: approx. € 78 million (PY: € 65.9 million)
  • Net income: approx. € 48 million (PY: € 33.3 million)

Berlin, 29 January 2026. According to preliminary, unaudited figures for the 2025 financial year, Eckert & Ziegler SE (ISIN DE0005659700, TecDAX) generated sales of around € 312 million and adjusted EBIT of around € 78 million. Sales are up around 5% on the previous year, while adjusted EBIT is up by around 18%. Net profit (from continuing and discontinued operations), which is only reported here for comparison purposes, rose to around € 48 million (previous year: € 33.3 million).

The forecast for the 2026 financial year will be published on 26 March 2026 together with the complete, audited annual financial statements for the 2025 financial year.

About Eckert & Ziegler.
Eckert & Ziegler SE with more than 1.000 employees is a leading specialist for isotope-related components in nuclear medicine and radiation therapy. The company offers a broad range of services and products for the radiopharmaceutical industry, from early development work to contract manufacturing and distribution. Eckert & Ziegler shares (ISIN DE0005659700) are listed in the TecDAX index of Deutsche Börse.
Contributing to saving lives.

Your contact:
Eckert & Ziegler SE, Karolin Riehle, Investor Relations
Robert-Rössle-Str. 10, 13125 Berlin, Germany
Tel.: +49 (0) 30 / 94 10 84-138, karolin.riehle@ezag.de, www.ezag.com 


29.01.2026 CET/CEST Dissemination of a Corporate News, transmitted by EQS News – a service of EQS Group.
The issuer is solely responsible for the content of this announcement.

The EQS Distribution Services include Regulatory Announcements, Financial/Corporate News and Press Releases.


Language: English
Company: Eckert & Ziegler SE
Robert-Rössle-Str.10
13125 Berlin
Germany
Phone: +49 30 941084-138
Fax: +49 30 941084-0
Internet: www.ezag.de
ISIN: DE0005659700
WKN: 565970
Indices: SDAX, TecDax,
Listed: Regulated Market in Frankfurt (Prime Standard); Regulated Unofficial Market in Dusseldorf, Hamburg, Munich, Stuttgart, Tradegate BSX
EQS News ID: 2268106

 
End of News EQS News Service

2268106  29.01.2026 CET/CEST

Lonza Delivers Strong Profitable Growth in Full-Year 2025 and Successfully Completes Vacaville Site Integration

  • In 2025, Lonza1 delivered sales of CHF 6.5 billion with +21.7% CER2 growth, and a CORE EBITDA of CHF 2.1 billion at a margin of 31.6% (+1.4ppts versus prior year), outperforming its upgraded CDMO outlook for the year
  • The strong momentum in winning new business continued in 2025 across Technology Platforms and sites, including a fifth significant commercial contract for Vacaville
  • The new One Lonza operating model was successfully launched on 1 April 2025 and already brings benefits for customers and operational performance
  • The proposed dividend of CHF 5.00 per share represents an increase of +25% versus prior year
  • For 2026, Lonza anticipates CER sales growth of 11-12% and further CORE EBITDA margin expansion, reaching a level above 32%
  • Capsules & Health Ingredients (CHI) saw +3.9% CER growth in 2025 and CORE EBITDA margin improvement of +1.6ppts versus prior year to 25.9%.3 CHI reported as Discontinued Operations

Basel, Switzerland, 28 January 2026 – Lonza1 reported sales of CHF 6.5 billion in FY 2025, reflecting a CER sales growth of +21.7% (+19.2% AER4) compared to prior year. A CORE EBITDA of CHF 2.1 billion resulted in a strong margin of 31.6% (+1.4ppts versus prior year), supported by maturing growth projects, robust operational execution and operating leverage. Excluding the business related to the Vacaville site, organic CER sales growth was in the low-teens at an improved CORE EBITDA margin, in line with Lonza’s CDMO Organic Growth Model.5

Lonza’s sales in 2025 benefited from robust momentum in the Mammalian, Bioconjugates, Small Molecules, Drug Product and Bioscience Technology Platforms, and was further supported by a higher than expected contribution of the Vacaville site. This was partially offset by a softer performance in Cell & Gene (CG) and phasing in Microbial.

Strategic, Operational and Organizational Progress in 2025

2025 was a year of significant progress for Lonza. On 1 April 2025, the company successfully implemented its new simplified and streamlined operating model, designed to deploy the new One Lonza strategy through three aligned Business Platforms (Integrated Biologics, Advanced Synthesis, Specialized Modalities) and strengthened cross‑platform Group Functions, especially in Operations and Quality. The organizational changes were executed seamlessly and are already improving ways of working, reflected in the strongly supportive feedback from Lonza’s leadership community in Voice of Employee surveys.

The establishment of a group‑wide Strategic Enterprise Account Management team further strengthened customer proximity, reflected in a significant uplift in Lonza’s already industry‑leading net promoter score versus prior year. The newly formed team for corporate strategy, innovation and M&A is focused on driving value creation as a pure‑play CDMO through organic and inorganic growth across current and future Technology Platforms. In parallel to these efforts, Lonza has continued to advance the CHI carve‑out and exit process as planned.

Overall, the ongoing transformation will further elevate Lonza’s ability to deliver a seamless customer experience at high service levels across all Business Platforms, improve manufacturing productivity, and efficiently execute growth projects in all key regions globally. This will ensure consistent, long‑term profitable growth in line with Lonza’s CDMO Organic Growth Model.

Business Highlights in 2025

Business highlights in 2025 included strong order momentum across Technology Platforms and sites. This included an increasing number of integrated drug substance-drug product agreements for clinical and commercial programs. Continuing strong customer interest in the Vacaville large-scale mammalian drug substance facility is evidenced by a fifth significant commercial contract and further contracts in late-stage negotiations. The Vacaville site is now fully integrated into Lonza’s global manufacturing network, including a seamless post‑merger integration, the first successful technical transfer of a new commercial product, the first successful US FDA audit under Lonza ownership, the first investments in operational flexibility well underway, and substantial new business already contractually secured.

With CHF 1.3 billion of CapEx in 2025 (19.6% of sales), Lonza made significant progress in executing its ongoing organic investment program to enable future growth across technologies, while gradually reducing its CapEx intensity. Strategic growth projects across Mammalian, Drug Product, Bioconjugates and CG progressed well and will provide the capacities and capabilities needed to drive long-term value creation, strengthening Lonza’s global CDMO market leadership.

The CHI business delivered on its Outlook 2025 with CER sales growth of +3.9% versus prior year, returning to a robust +8.0% CER sales growth in H2 2025. The CORE EBITDA margin improved by +1.6ppts to 25.9% in FY 2025. Going forward, recent final affirmative determinations in US antidumping and countervailing investigations are expected to restore competitive balance to the benefit of future growth and margins. Following a well-executed carve‑out process, CHI as a Discontinued Operation delivered +4.4% CER growth at a CORE EBITDA margin of 24.7%.

Sustainability and Governance

Lonza is on track to achieve its 2023 science-based near-term sustainability targets, including its commitment to reduce absolute Scope 1 and 2 greenhouse gas (GHG) emissions by 42% by 2030.6 In 2025, the company achieved reductions of more than 50% in both GHG and waste intensity against the 2018 base year, surpassing both 2030 targets ahead of plan. Lonza continued to expand renewable sourcing across all key regions. As of January 2026, all electricity purchased across the US, Europe and China is now from renewable sources.

In October 2025, Lonza’s Board of Directors announced the nomination of Claudia Süssmuth-Dyckerhoff as an Independent Member and Vice-Chair of the Board of Directors, subject to her election at the AGM in May 2026. Claudia brings a wealth of international experience in healthcare and life sciences, and an outstanding track record of board memberships in publicly listed companies.

Lonza’s Board of Directors will propose to increase the dividend by +25% to CHF 5.00 per share at the Lonza AGM in May 2026. Subject to approval, 50% of the dividend will be paid out of the capital contribution reserve, meaning it will be exempt from Swiss withholding tax.

Wolfgang Wienand, CEO, Lonza, commented: “2025 was a strong year for the One Lonza team, marked by significant revenue growth with expanding profitability alongside tangible progress on our transformation journey. We executed our existing business with rigor and, at the same time, continued to lay the foundations for future growth. In the face of geopolitical and economic volatility, Lonza’s business model, once again, proved resilient and delivered on the promise to effectively diversify risks across the broadest technology offering, commercial portfolio and global manufacturing footprint in the CDMO industry. Based on what we achieved together in 2025, we are well positioned to continue executing our strategy in 2026 and beyond – for the benefit of our customers and their patients, our shareholders and our people.”

Outlook 2026

For 2026, Lonza anticipates a continued strong performance in line with its CDMO Organic Growth Model and expects CER sales growth of 11-12% and further CORE EBITDA margin expansion, reaching a level above 32% of sales. CER sales growth is expected to be stronger in the first half of 2026 than in the second half.

Lonza anticipates an FX7 headwind of approximately -2.0% on sales and CORE EBITDA in 2026, mainly from the full-year effect of the weakening of the US Dollar in 2025, assuming spot rates of mid-January 2026 prevail throughout the year. With a robust natural hedge and Lonza’s financial hedging program, margins will be minimally impacted.

Given recent geopolitical and geoeconomic shifts toward more regional supply chains and its extensive and well‑diversified global manufacturing network across key regions and technologies, Lonza is well positioned to support customers seeking to align regional supply with regional demand. Looking ahead, Lonza plans to further expand its asset base, leveraging its strong track record of building, acquiring, and operating assets worldwide. The high‑quality, large‑scale capacities in Vacaville, together with the expertise of its local team, significantly strengthens Lonza’s global mammalian offering. As the largest biologics CDMO in the US, Lonza is uniquely positioned to support customers looking to align US supply with US demand.

The significant investment announcements of large pharmaceutical companies are likely to be primarily shifts in global CapEx spend toward the US, while biotech companies continue to have a limited focus on in-house capacities. The strong economic rationale to outsource to CDMOs remains unchanged for large pharma and biotech companies to enable economically efficient global pharmaceutical supply.

In the evolving geopolitical and geoeconomic landscape, Lonza expects no material financial impact from currently published US trade and tariff policies but continues to monitor the situation closely.

For its CHI business in 2026, Lonza expects mid-single-digit percentage CER sales growth and further CORE EBITDA margin expansion.

Business Platform Overview for 2025: Continuing Business

  • Integrated Biologics reported strong CER sales growth of +32.2% versus prior year, driven by sustained demand for its large-, mid-, and small-scale assets, supported by maturing growth projects and the Vacaville site acquisition, which generated around CHF 0.6 billion sales. The CORE EBITDA margin reached 35.3% (-0.9ppts versus prior year) with good operational execution almost offsetting the dilution from growth projects and unfavorable portfolio mix effects.
  • Advanced Synthesis reported exceptionally strong CER sales growth of +22.4% versus prior year, supported by rapid and simultaneous ramp-up of recently added growth projects in Small Molecules and Bioconjugates. Good operational execution, efficient growth project ramp-ups and operating leverage led to a CORE EBITDA margin of 41.8% in FY 2025 (+5.2ppts versus prior year).
  • Specialized Modalities reported a CER sales decline of -3.0%versus prior year, impacted by a softer operational performance in CG and phasing in Microbial. Compared to a weaker H1 2025, the business showed improving trends with H2 returning to growth, especially in Microbial, while CG remained subdued. Bioscience reported robust CER sales growth throughout the year. The Platform’s CORE EBITDA margin remained almost unchanged at 17.0% (-0.5ppts versus prior year), driven by favorable portfolio mix effects and cost discipline.
 

Group Financial Summary for 2025: Continuing Business

CHF million

 

FY 2025

 

YoY change (in %)

 

FY 2024

Sales in AER

 

6,531

 

+19.2

 

5,480

Growth in CER in %

 

+21.7

 

+20.4ppts

 

+1.3

CORE EBITDA

 

2,064

 

+24.9

 

1,653

    Margin in %

 

31.6

 

+1.4ppts

 

30.2

EBITDA

 

1,970

 

+35.7

 

1,452

    Margin in %

 

30.2

 

+3.7ppts

 

26.5

EBIT

 

1,239

 

+36.5

 

908

    Margin in %

 

19.0

 

+2.4ppts

 

16.6

For more details, please refer to the Full-Year 2025 Presentation, Full-Year 2025 Report and Alternative Performance Measures (APM) 2025 Report.


1 Financial information presented for “Lonza” reflects Lonza’s continuing CDMO business.
2 Constant Exchange Rates (CER).
3 Excluding costs directly attributable to Discontinued Operations. See page 41 of the FY 2025 presentation for a bridge to Discontinued Operations.
4 Actual Exchange Rates (AER).
5 Low-teens organic CER sales growth on average over time and CORE EBITDA growth ahead of sales growth.
6 Against the 2021 base year.
7 Foreign Exchange.

MHH to Present Scientific Findings on Cold Plasma Therapy for Pulmonary Application at Press Conference in February 2026

Viromed Medical AG

/ Key word(s): Miscellaneous

MHH to Present Scientific Findings on Cold Plasma Therapy for Pulmonary Application at Press Conference in February 2026

27.01.2026 / 16:43 CET/CEST

The issuer is solely responsible for the content of this announcement.


PRESS RELEASE

MHH to Present Scientific Findings on Cold Plasma Therapy for Pulmonary Application at Press Conference in February 2026

Rellingen, 27 January 2026 – On 12 February 2026, Hannover Medical School (MHH) – represented by Prof. Dr. Hortense Slevogt – plans to hold a press conference together with the team from the Helmholtz Centre for Infection Research (HZI) in Braunschweig.

The focus of the event will be the presentation and scientific classification of a groundbreaking cold plasma therapy for application in the lungs. For Viromed stakeholders, the findings are of high strategic relevance, as they address a medical field in which there is an urgent and, to date, insufficiently met clinical need worldwide: severe pulmonary infections – particularly in vulnerable patient groups and in intensive care settings.

The relevance of the topic is driven in particular by three key factors:

  • High global disease burden: Pulmonary infections and associated complications affect millions of patients worldwide every year and represent one of the major challenges of modern acute and intensive care medicine.
  • Growing therapeutic limitations: The increasing prevalence of antibiotic-resistant pathogens further exacerbates the situation and intensifies the pressure to develop new and effective therapeutic approaches.
  • New physical treatment option: The planned publication of an innovative physical therapy principle for the lungs potentially represents a paradigm shift in infection treatment and opens up the prospect of scalable clinical application.

 

About Viromed Medical AG

Viromed Medical AG specializes in the development, manufacture and distribution of medical products. The operating business of the company, which has been listed on the stock exchange since October 2022, focuses on the distribution of innovative cold plasma technology for medical applications via its wholly owned subsidiary Viromed Medical GmbH. Viromed can draw on a broad customer base in the DACH region and beyond. Viromed is pursuing the goal of further advancing the use of cold plasma technology in medicine in the coming years and realizing the corresponding growth potential.

www.viromed-medical-ag.de

Contact Viromed

E-Mail: kontakt@viromed-medical.de
 

Press contact

E-mail: viromed@kirchhoff.de


27.01.2026 CET/CEST Dissemination of a Corporate News, transmitted by EQS News – a service of EQS Group.
The issuer is solely responsible for the content of this announcement.

The EQS Distribution Services include Regulatory Announcements, Financial/Corporate News and Press Releases.


Language: English
Company: Viromed Medical AG
Hauptstraße 105
25462 Rellingen
Germany
E-mail: kontakt@viromed-medical.de
Internet: https://www.viromed-medical-ag.de/
ISIN: DE000A40ZVN7
WKN: A40ZVN
Listed: Regulated Unofficial Market in Dusseldorf, Frankfurt, Hamburg, Tradegate BSX
EQS News ID: 2266836

 
End of News EQS News Service

2266836  27.01.2026 CET/CEST

Siegfried to acquire high-quality small molecules drug substance capacity in the US

Media Release
Zofingen, January 27, 2026

Ad hoc announcement pursuant to Art. 53 Listing Rules

Siegfried (SIX: SFZN), a leading global Contract Development and Manufacturing Organization (CDMO) for the pharmaceutical industry, has signed binding agreements with an affiliate of SK Capital Partners to acquire the drug substance business of the Noramco Group and Extractas Bioscience. The acquired businesses include three high-quality small molecules drug substances sites with approximately 400 employees:

  • Noramco, a large, commercial-scale manufacturing site in Wilmington, Delaware (US)
  • Purisys, a clinical API development and manufacturing facility located in Athens, Georgia (US)
  • Extractas Bioscience, a leading manufacturer of purified products based in Westbury, Tasmania (AU)

The acquisition marks another important milestone in the execution of Siegfried’s EVOLVE+ strategy, expanding the company’s presence and capacity in the US, the world’s largest pharmaceutical market.

Siegfried plans to expand its fast-growing exclusive synthesis business in the US by optimizing its controlled substance capacity across the newly acquired Wilmington site and its nearby Pennsville site. Combined with the early-phase development capabilities of Purisys and the extraction expertise of Extractas Bioscience, the acquisition strengthens Siegfried’s integrated offering to its customers and provides a strong foundation for accelerating growth and improving profitability.

Marcel Imwinkelried, Chief Executive Officer: “This transaction marks a decisive next step in the execution of our EVOLVE+ strategy and is aligned with our highly selective, disciplined value accretive approach to M&A. By adding exceptional US-based capabilities, we will become even more attractive to both existing and new customers, creating new opportunities to accelerate profitable growth. The combined capacity and expertise of the three sites strengthen our position as a leading CDMO for small-molecule drug substances, and I look forward to fully realizing this value together with our new colleagues.”  

The valuation of the acquired business is below 10 times Enterprise Value / EBITDA. Given Siegfried’s strong balance sheet, the acquisition will be financed through existing and new debt instruments. Subject to customary closing conditions, the transaction is expected to close later this year.

DocMorris repurchases convertible bonds maturing in 2026 with a nominal value of around CHF 14.4 million

DocMorris AG

/ Key word(s): Bond

DocMorris repurchases convertible bonds maturing in 2026 with a nominal value of around CHF 14.4 million

26.01.2026 / 18:30 CET/CEST


Frauenfeld, 26 January 2026

Press release

DocMorris repurchases convertible bonds maturing in 2026 with a nominal value of around CHF 14.4 million

DocMorris Finance B.V. has agreed with a holder of 2026 convertible bonds to purchase an aggregate nominal amount of around CHF 14.4 million. The purchase is expected to be settled in the coming days. The completion of the purchase and the immediate cancellation will reduce the total outstanding aggregate nominal amount to less than CHF 8.0 million from the original CHF 95.0 million.

 

Investors and analyst contact
Lisa Lüthi, Senior Investor Relations Manager
Email: ir@docmorris.com

Media contact
Torben Bonnke, Director Communications
Email: media@docmorris.com, phone: +49 171 864 888 1

Agenda

19 March 2026 2025 Full-year results and outlook 2026 (Zurich / hybrid)
16 April 2026 Q1/2026 Trading update
12 May 2026 Annual General Meeting, Zurich
19 August 2026 2026 Half-year results (conference call/webcast)
15 October 2026 Q3/2026 Trading update

 

DocMorris
The Swiss-based DocMorris AG is a leading company in the fields of online pharmacy, telemedicine and marketplace with strong brands in Germany and other European countries. Deliveries are mainly from the highly automated logistics centre in Heerlen, the Netherlands. TeleClinic is Germany’s largest telemedicine platform, connecting patients with more than 6,000 physicians. DocMorris operates leading marketplaces for health and personal care products in Southern Europe. With its broad range of products and services, DocMorris is pursuing its vision of becoming the leading digital health companion for everyone to manage their health in one click. Around 1,600 employees in Germany, the Netherlands, Spain, France, Portugal and Switzerland generated an external revenue of CHF 1,186 million serving 11 million active customers in 2025. The shares of DocMorris AG are listed on the SIX Swiss Exchange (securities number 4261528, ISIN CH0042615283, ticker DOCM). For further information, please visit corporate.docmorris.com.

 


End of Media Release


Language: English
Company: DocMorris AG
Walzmühlestrasse 49
8500 Frauenfeld
Switzerland
ISIN: CH0042615283
Listed: SIX Swiss Exchange
EQS News ID: 2266206

 
End of News EQS News Service

2266206  26.01.2026 CET/CEST

Dr. Christian Schlögel nominated as new member of the Board of Directors

SKAN AG

/ Key word(s): Personnel

Dr. Christian Schlögel nominated as new member of the Board of Directors

26.01.2026 / 17:45 CET/CEST


Media Information

Dr. Christian Schlögel nominated as new member of the Board of Directors

Allschwil, January 26, 2026 – The Board of Directors of SKAN Group AG proposes Dr. Christian Schlögel as a new member for election at the Annual General Meeting on May 7, 2026. Patrick Schär will not stand for re-election after 16 years on the Board of Directors.

Dr. Christian Schlögel (born 1964, German citizen) is a proven expert in software, digital transformation and artificial intelligence with 30 years of leadership experience in global technology, software and industrial companies. From 2018 to 2025, he was Group Chief Digital Officer and member of the Executive Board of Körber AG, where he was responsible for the digital transformation of the group with around 14,000 employees. From 2014 to 2018, he was Group Chief Technology & Digital Officer at KUKA AG, an international automation and robotics group with around 15,000 employees. He currently contributes his expertise as a member of administrative and advisory boards at various companies. Christian Schlögel started his professional career at SAP AG. He holds a degree in computer science from the Karlsruhe Institute of Technology and a doctorate in business administration from the University of Passau.

Beat Lüthi, Chairman of the Board of Directors of the SKAN Group, explained: “SKAN expands its offering to include software and digital integration services, for which we acquired a majority stake in Metronik last year. In parallel, we are driving forward the digital transformation of the company and our services. Christian Schlögel can significantly support these initiatives, which are core elements of the strategy for future sales and margin growth, with his expertise. The Board of Directors is therefore delighted to be able to propose him for election to the shareholders.

Patrick Schär has decided not to stand for re-election to the Board of Directors for professional reasons. Beat Lüthi added: “Patrick Schär has been on the Board of Directors for 16 years. With his professional background and experience as a financial expert, he has made a significant contribution to the development of the SKAN Group. We would like to thank him sincerely for his many years of commitment and the excellent collaboration and wish him all the best for his professional and personal future.”

 

Contacts:

Thomas Balmer, ir@skan.com, +41 79 703 87 28
Alexandre Müller, ir@skan.com, +41 79 635 64 13

 

Financial calendar:

24 March 2026 Publication Annual Results 2025
7 May 2026 Annual General Meeting 2026

 

SKAN – together always one step ahead
SKAN is a pioneer in the field of aseptic and aseptic-toxic manufacturing processes for the (bio)pharmaceutical industry. The company is the market and technology leader for high-quality, process-critical isolator systems for filling drugs according to strict sterility standards. In addition, the company offers its customers process support, services and consumables. Innovative solutions and an efficient life-cycle support organisation make SKAN an important partner for the pharmaceutical and biotech industry, CMOs (Contract Manufacturing Organisations) and research laboratories worldwide. Founded in 1968, SKAN today employs close to 1700 people. More than half of them work at the Allschwil headquarters in the Life Sciences Hub of the Basel region. The other employees are located among the subsidiaries in Switzerland, Germany, Belgium, France, Slovenia, Croatia, Japan, the USA and Brazil.

 


End of Media Release


Language: English
Company: SKAN AG
Kreuzstrasse 5
4123 Allschwil
Switzerland
Phone: +41 43 268 32 32
E-mail: info@skan.com
ISIN: CH0013396012
Valor: 1339601
Listed: SIX Swiss Exchange
EQS News ID: 2265850

 
End of News EQS News Service

2265850  26.01.2026 CET/CEST

SKAN announces preliminary key figures for the 2025 financial year

SKAN AG / Key word(s): Annual Results

SKAN announces preliminary key figures for the 2025 financial year

26-Jan-2026 / 07:00 CET/CEST

Release of an ad hoc announcement pursuant to Art. 53 LR

The issuer is solely responsible for the content of this announcement.


Ad hoc announcement pursuant to Art. 53 LR

SKAN announces preliminary key figures for the 2025 financial year

Allschwil, January 26, 2026 – The SKAN Group AG, world market leader for high-quality isolator systems for aseptic production processes in the pharma and biotech industry, expects based on preliminary, not yet audited figures net sales of around CHF 332 million (2024: CHF 361.3 million) and earnings before interest, taxes, depreciation and amortization (EBITDA) of around CHF 38 million (2024: CHF 57.0 million). Order intake is expected to reach around CHF 365 million (2024: CHF 359.5 million).

Publication of the 2025 financial results:

SKAN Group AG will publish the detailed 2025 financial results on Tuesday, March 24, 2026, at 7:00 a.m. At the same time, the 2025 Annual Report and the 2025 year-end presentation will be available for download at www.skan.com. An investor, analyst and media conference is also planned for 10:00 a.m. at the Widder Hotel in Zurich. Further details will be provided in due course.

 

Contacts:

Thomas Balmer, ir@skan.com, +41 79 703 87 28
Alexandre Müller, ir@skan.com, +41 79 635 64 13

 

Financial calendar:

24 March 2026 Publication Annual Results 2025
7 May 2026 Annual General Meeting 2026

 

SKAN – together always one step ahead
SKAN is a pioneer in the field of aseptic and aseptic-toxic manufacturing processes for the (bio)pharmaceutical industry. The company is the market and technology leader for high-quality, process-critical isolator systems for filling drugs according to strict sterility standards. In addition, the company offers its customers process support, services and consumables. Innovative solutions and an efficient life-cycle support organisation make SKAN an important partner for the pharmaceutical and biotech industry, CMOs (Contract Manufacturing Organisations) and research laboratories worldwide. Founded in 1968, SKAN today employs close to 1700 people. More than half of them work at the Allschwil headquarters in the Life Sciences Hub of the Basel region. The other employees are located among the subsidiaries in Switzerland, Germany, Belgium, France, Slovenia, Croatia, Japan, the USA and Brazil.

 


End of Inside Information


Language: English
Company: SKAN AG
Kreuzstrasse 5
4123 Allschwil
Switzerland
Phone: +41 43 268 32 32
E-mail: info@skan.com
ISIN: CH0013396012
Valor: 1339601
Listed: SIX Swiss Exchange
EQS News ID: 2265492

 
End of Announcement EQS News Service

2265492  26-Jan-2026 CET/CEST

Rentschler Biopharma appoints Detra Glinatsis as Head of Business Development U.S.

Rentschler Biopharma SE

/ Key word(s): Personnel

Rentschler Biopharma appoints Detra Glinatsis as Head of Business Development U.S.

22.01.2026 / 13:00 CET/CEST

The issuer is solely responsible for the content of this announcement.


 Rentschler Biopharma appoints Detra Glinatsis as Head of Business Development U.S.

Laupheim (Germany), Milford, MA (USA), January 22, 2026 – Rentschler Biopharma SE, a leading global contract development and manufacturing organization (CDMO) for biopharmaceuticals, today announced that Detra Glinatsis has rejoined the company as Head of Business Development U.S. In this newly created role, Ms. Glinatsis will lead all business development activities related to the U.S. market. She reports to Dr. Patrick Meyer, Global Head of Business Development, and is based at the company’s site in Milford, MA.

Dr. Patrick Meyer, Global Head of Business Development at Rentschler Biopharma, commented: “I am excited to have Detra rejoin Rentschler Biopharma to serve in this important role. Her career is a true testament to her expertise, client‑centric mindset, and ability to build long‑lasting, meaningful partnerships. The United States is a cornerstone of our commercial strategy, and our presence in Milford, MA enables us to bring Rentschler Biopharma’s innovative thinking and development strength directly to the doorstep of our clients. In the past two years, we have successfully transferred one post‑PPQ[] commercial program to the site, are advancing three additional programs toward PPQ, and initiated manufacturing for six new products in 2025 – clear proof of the momentum Detra will now help to accelerate. Expanding our U.S. business is critical to the next growth stage of our corporate strategy, and Detra, with her commitment to excellence and exceeding client expectations, is the ideal person to lead our U.S. business development activities.”

Detra Glinatsis brings over twenty years of sales and business development experience in the pharmaceutical, biotech and contract manufacturing industries. She rejoins Rentschler Biopharma from Northway Biotech, where she was Vice President, Business Development. She previously held roles of increasing responsibility at AGC Biologics, Sartorius, Gallus BioPharmaceuticals, and Avecia Biologics, as well as Rentschler Biopharma, where, earlier in her career, she was Senior Director, Business Development. Ms. Glinatsis holds a B.S. in biology from the University of Akron.

Detra Glinatsis, Head of Business Development U.S., said: “I am thrilled to come back to Rentschler Biopharma as the company continues to grow its U.S. business. Together with the team, I look forward to building on the success that the company has achieved with the Milford site expansion and continuing to enhance the Rentschler Biopharma brand in the U.S. The company has a long-standing reputation for top quality and reliability, and I am excited to be working with such a talented team with a coveted track record.”

About Rentschler Biopharma SE

Rentschler Biopharma is a leading contract development and manufacturing organization (CDMO) focused exclusively on client projects. The company offers process development and manufacturing of biopharmaceuticals as well as related consulting activities, project management and regulatory support. Rentschler Biopharma’s high quality is proven by its long-standing experience and excellence as a solution partner for its clients. A high-level quality management system, a well-established operational excellence philosophy and advanced technologies ensure product quality and productivity at each development and manufacturing step. Rentschler Biopharma is a family-owned company with about 1,400 employees, headquartered in Laupheim, Germany, with operations in Milford, MA, USA. In 2024, the company joined the United Nations Global Compact, emphasizing Rentschler Biopharma’s focus on sustainability. For further information about the company, please visit www.rentschler-biopharma.com. Follow Rentschler Biopharma on LinkedIn.

Contact:
Rentschler Biopharma SE

Dr. Latika Bhonsle-Deeng
Global Head of Communications
Phone: +49-7392-701-467
communications@rentschler-biopharma.com

Media inquiries:
MC Services AG

Phone: +49-89-210228-0
rentschler@mc-services.eu

U.S.
Laurie Doyle
Phone: +1-339-832-0752

For high-resolution images, please contact communications@rentschler-biopharma.com.

[] PPQ = Process Performance Qualification


22.01.2026 CET/CEST Dissemination of a Corporate News, transmitted by EQS News – a service of EQS Group.
The issuer is solely responsible for the content of this announcement.

The EQS Distribution Services include Regulatory Announcements, Financial/Corporate News and Press Releases.


2264578  22.01.2026 CET/CEST