Q2 and H1 2026 Trading Update
Shield Therapeutics plc reported Q2 2026 revenues of $11.9 million, with ACCRUFeR® revenues reaching $10.3 million, and announced first half revenues of $30.4 million, a significant increase from $21.5 million in H1 2025, driven by a development milestone payment and higher partner royalties, leading to profitability in H1 2026. The company also saw a 21% growth in prescriptions dispensed in H1, with approximately 102,000 dispensed, and has appointed Michael Jensen as Chief Financial Officer, effective September 1, 2026, as they remain on track for profitability in 2026.
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On track for profitability in 2026
New CFO, Michael Jensen joins the Company on 1 September 2026
London, UK, 30 July 2026: Shield Therapeutics plc (LSE: STX), a commercial-stage pharmaceutical company focused on iron deficiency, today releases its unaudited Q2 and H1 2026 trading update and announces the appointment of Michael Jensen as Chief Financial Officer.
In Q2 2026, unaudited Group net revenues were $11.9M. ACCRUFeR® revenues continue to grow to $10.3M. Following the changes introduced to the Prior Authorisation (PA) requirements for prescription approvals in the Medicaid program in New York, the Company quickly pivoted to focus on commercial business outside of Medicaid. This resulted in the Company achieving 27% growth in H1 2026 compared to H1 2025, with the month of June growing 6% month over month.
Shield is delighted to announce the appointment of Michael Jensen as Chief Financial Officer, joining the Company on September 1, 2026. Michael brings more than 20 years of executive financial leadership experience across the biopharmaceutical, medical device, and healthcare sectors, with a strong track record of driving financial and operational transformation in both public and venture capital-backed organisations, supporting commercial growth, strengthening financial performance, and creating shareholder value. Michael joins Shield from StimLabs, where he served as Chief Financial Officer, and previously held CFO positions at Synlogic and Intrinsic Therapeutics. Earlier in his career, he held senior finance leadership roles at Novo Nordisk, Novartis, and Siemens Healthcare Diagnostics. Michael holds a Master's degree from Copenhagen Business School, including studies in the MBA program at Duke University's Fuqua School of Business, and an undergraduate degree from Towson University, Maryland.
Q2 and H1 2026 Key Business Metrics:
- H1 2026 total revenues increased to $30.4M vs ($21.5M in H1 2025) driven by the achievement of the $7.9M development milestone payment by ASK in China and higher partner royalties, resulting in the Company remaining profitable during H1 2026. Q2 Group net revenue of $11.9M, (Q2 2025: $14.3M).
- ACCRUFeR® sales in the US:
o ACCRUFeR® net revenues of $10.3M (Q2 2025: $12.8M) with an average net price of $208 (Q2 2025: $231) influenced by the PA requirements in NY
o Increased prescriptions dispensed with c.49,000 in Q2 2026 (c.47,000 in Q2 2025)
o Growth of 21% in prescriptions dispensed in H1 with c.102,000 (c.84,000 in H1 2025)
o Cash and cash equivalents of $8.3M as of 30 June 2026 compared to $12.4M on 31 March 2026 primarily driven by working capital and cost management
- First GPO (Group Purchasing Organisation) contract signed. New opportunity to market and sell ACCRUFeR® to 400+ clinics.
Global regulatory and pipeline progression:
- MEDLEAP Pharma, a subsidiary of Vital KSK Holdings Inc. confirmed its first patient enrollment for the Phase II clinical trial for ACCRUFeR® (ferric maltol), a new drug candidate for Pulmonary Arterial Hypertension (PAH), for patients in Japan. This clinical trial is an exploratory study intended to support a planned Phase III trial. It follows the Pharmaceuticals and Medical Devices Agency's (PMDA) confirmation of the development plan for the drug as a PAH treatment in Japan, based on the drug's prior clinical results from trials in Europe, the UK, and the USA.
- Norgine (UK & EU): Indication extension to include pediatric patients 12 years of age and older. The European Medicines Agency (EMA) positive opinion in Europe was received on 26 March 2026, followed by the European Commission's (EC) Decision on 26 May 2026. The Medicines and Healthcare products Regulatory Agency's (MHRA) approval in the UK was received on 2 July 2026.
- Launch of the Indication extension for pediatric patients 10 years of age and older was received in the US on 1 April 2026.
- Attendance at BIO-Europe and BIO US generated productive conversations with potential partners around assets suitable for US in-licensing, supporting Shield's commercialisation strategy.
- Publication of a report in Pediatric Drugs, reinforcing FDA approval. This report, titled Ferric Maltol: Pediatric First Approval, is available via the following link:https://link.springer.com/article/10.1007/s40272-026-00748-3
Anders Lundstrom, Chief Executive Officer, commented: "We are pleased with the significant growth in our largest business segment, commercial, which represents two-thirds of total revenue, alongside strong overall prescription growth. Our prior experience in Texas, pivoting from Medicaid to commercial, gives us confidence in this strategy. I am also excited to welcome Michael Jensen as our new CFO. His experience will strengthen our leadership team and support the financial and operational transformation as we drive toward profitability in 2026".
Investor Presentation
Anders Lundstrom, Chief Executive Officer, Andy Hurley, Chief Commercial Officer, and Bryon Kallert, Senior Director, Financial Planning & Analysis, will be hosting a live webinar relating to the Q2 & H1 2026 Trading Update at 2:15 pm (BST) on 30 July 2026. Questions can be submitted pre-event via your Investor Hub dashboard up until 2.15 pm (BST) on 30 July 2026 or at any time during the live presentation.
How to sign up for the Shield Therapeutics plc Investor Hub:
- Visit shieldtherapeutics.com
- Follow the prompts to sign up for an Investor Hub account
- Complete your account profile
To access the webinar please visit: https://shieldtherapeutics.com/webinars
Clinically low iron levels (aka iron deficiency, ID) can cause serious health problems for children and adults of all ages, across multiple therapeutic areas. Together, ID and ID with anemia (IDA) affect about 20 million people in the US and represent a $2.3B market opportunity. As the first and only FDA approved oral iron to treat ID/IDA, ACCRUFeR® has the potential to meet an important unmet medical need for both physicians and patients and is now the #1 branded prescription oral iron in the US market today (*data source - IQVIA Xponent PlanTrak).
Cleaned text: letterheads, contacts and legal notices removed. View the original announcement ↗ · Company filings. Not investment advice.