Hemogenyx Pharmaceuticals H1 2026 Results: Loss widens to £6.56m, cash at £4.58m
- Loss before taxation widened to £6,557,736 in H1 2026 from £5,006,415 in H1 2025
- Non-cash share-based payment charge of £5,543,473 drove the increase in reported losses
- Cash and cash equivalents stood at £4,584,849 as of June 30, 2026
- Company raised £5.6 million in gross proceeds during the first half of 2026
- Signed definitive collaboration agreement with Cellin Technologies for Estonian market

*this image is generated using AI for illustrative purposes only.
Hemogenyx Pharmaceuticals plc (LSE: HEMO) recorded a loss before taxation of £6,557,736 for the six months ended June 30, 2026, up from £5,006,415 in the prior year period. The increase was primarily driven by a non-cash share-based payment charge of £5,543,473, while underlying operating costs declined compared to the same period in 2025.
The company raised £5.6 million in gross proceeds during the first half of 2026 to support ongoing clinical development. As of June 30, 2026, Hemogenyx held cash and cash equivalents totalling £4,584,849. The biopharmaceutical group continues to advance its lead candidate, HG-CT-1, an autologous CAR-T therapy for relapsed or refractory acute myeloid leukaemia (AML).
Clinical and operational milestones
Hemogenyx submitted its second Annual Investigational New Drug (IND) Report to the FDA for HG-CT-1, covering data from three adult patients treated at the initial dose level. The report indicated that CAR-T cell expansion and persistence were observed in all subjects, with peak levels occurring between 14 and 28 days post-infusion. No immune effector cell-associated neurotoxicity syndrome (ICANS) or dose-limiting toxicities were reported.
The company has completed the technology transfer of HG-CT-1 manufacturing to Made Scientific, reducing its operating cost base. This outsourcing decision is expected to lower the burn rate further in the current financial year. Additionally, Hemogenyx secured FDA clearance to initiate Phase I trials in paediatric patients, expanding the programme beyond adults.
Commercialisation partnerships
The company has established early commercialisation pathways in Europe through hospital exemption frameworks:
- Estonia: A definitive collaboration agreement was signed with Cellin Technologies OÜ on August 11, 2026. Cellin will serve as the exclusive manufacturing and operational partner for five years under Estonia’s Medicinal Products Act hospital exemption pathway.
- Lithuania: A letter of intent was signed with Vilnius University Hospital Santaros Klinikos on July 29, 2026, for translational research and compassionate-use treatment under Lithuania’s hospital exemption framework.
These arrangements aim to generate early revenues and real-world clinical data while full marketing authorisation is pursued. However, the company noted that revenue is contingent on successful technology transfer, regulatory authorisation, and reimbursement approvals.
Financial performance
| Metric | H1 2026 (£) | H1 2025 (£) | Change |
|---|---|---|---|
| Loss before taxation | 6,557,736 | 5,006,415 | Widened |
| Operating costs | 6,481,401 | 4,886,532 | Increased |
| Share-based payment charge | 5,543,473 | N/A | Non-cash |
| Cash and cash equivalents | 4,584,849 | N/A | Period end |
Excluding the non-cash share-based payment charge, operating costs were lower than in the comparative period, reflecting reduced underlying expenditure. The company emphasised financial discipline and resource management as key priorities for the remainder of 2026.
What the numbers show
The divergence between the widening statutory loss and the declining underlying operating costs highlights the impact of accounting charges versus cash burn. While the reported loss increased by approximately 31% year-on-year, the £5.54 million share-based payment charge accounts for the majority of this rise. Excluding this non-cash item, the company’s actual cash outflow for operations appears to have decreased, aligning with its stated strategy of outsourcing manufacturing to Made Scientific to manage burn rate. The £4.58 million cash position, combined with the £5.6 million raised during the period, provides near-term liquidity for clinical progression, though future capital needs remain dependent on trial outcomes and commercialisation milestones.
How will the transition to Made Scientific for manufacturing impact the projected cash burn rate and timeline for HG-CT-1's Phase I paediatric trials?
What specific regulatory milestones must Hemogenyx achieve in Estonia and Lithuania to convert hospital exemption revenues into sustainable commercial income?
Given the £4.6 million cash position, when is the next capital raise likely to occur to fund the expanded clinical programme through to pivotal trial stages?


























