AI assistant
IMMUPHARMA PLC — Regulatory Filings 2021
Aug 12, 2021
7703_iss_2021-08-12_e0600f06-fa98-4997-ad03-782acfa15e62.pdf
Regulatory Filings
Open in viewerOpens in your device viewer
12 August 2021
ImmuPharma PLC
("ImmuPharma" or the "Company")
FDA approves the Lupzuor™ PK study
ImmuPharma PLC (LSE:IMM) (Euronext Growth Brussels: ALIMM), the specialist drug discovery and development company, is delighted to announce that the US Food & Drug Administration ("FDA") has approved the commencement of the pharmacokinetic ("PK") study, as part of the new optimised international Phase 3 trial of Lupuzor™.
The PK study is a Phase I study to assess the presence of Lupuzor™ in the body after administration of a single dose. The study will be carried out in a total of up to 24 healthy male subjects. Dependent on timing of patient recruitment, we anticipate that the PK study will take between 8-12 weeks to complete, from commencement.
Preparations will be made to commence the Phase 3 study, following completion of the PK study. For the continued late-stage program development, ImmuPharma and Avion Pharmaceuticals LLC ("Avion"), as part of a joint steering committee, agreed on a collaborative group consisting of a Board of Key Opinion Leaders ("KOLs") and a leading medical patient advocacy group. Collectively, this network, due to its in-depth knowledge of the lupus disease and their access to lupus patient groups, will be invaluable to the successful outcome of the Phase 3 trial.
ImmuPharma will provide an update on the progress of the PK study once it has commenced.
Commenting on the announcement, Tim McCarthy, Chairman & CEO of ImmuPharma said: "We are extremely pleased to see the next positive steps for Lupuzor™, with continued positive dialogue with the FDA, their approval to commence the PK study and an agreed clinical and regulatory pathway over the next period. We look forward to providing further progress updates on the PK study and ultimately moving Lupuzor™ forward into the optimised Phase 3 study, on the successful completion of the PK study."
End
This announcement contains inside information as stipulated under the UK version of the Market Abuse Regulation no 596/2014 which is part of English law by virtue of the European (withdrawal) Act 2018, as amended. on publication of this announcement via a regulatory information service, this information is considered to be in the public domain.
For further information please contact:
| ImmuPharma PLC (www.immupharma.com) | + 44 (0) 207 152 4080 |
|---|---|
| Tim McCarthy, Chairman and Chief Executive Officer | |
| Dr Tim Franklin, Chief Operating Officer | |
| Lisa Baderoon, Head of Investor Relations | + 44 (0) 7721 413496 |
| SPARK Advisory Partners Limited (NOMAD) | +44 (0) 203 368 3550 |
| Neil Baldwin | |
| Stanford Capital Partners (Joint Broker) | +44 (0) 203 815 8880 |
| Patrick Claridge | |
| John Howes | |
| Bob Pountney | |
| SI Capital (Joint Broker) | +44 (0) 1483 413500 |
| Nick Emerson | |
| 4Reliance (Euronext Growth Listing Sponsor) | +32 (0) 2 747 02 60 |
| Jean-Charles Snoy | |
| Degroof Petercam (Liquidity Provider) | +32 (0) 2 287 95 34 |
| Erik De Clippel | |
| Backstage Communication | |
| Olivier Duquaine | +32 (0) 477 504 784 |
| Gunther De Backer | +32 (0) 475 903 909 |
Notes to Editors
About ImmuPharma PLC
ImmuPharma PLC (LSE AIM: IMM – Euronext Growth: ALIMM) is a specialty biopharmaceutical company that discovers and develops peptide-based therapeutics. The Company's portfolio includes novel peptide therapeutics for autoimmune diseases, metabolic diseases, anti-infectives and cancer. The lead program, Lupuzor™, is a first-in class autophagy immunomodulator which is in Phase 3 for the treatment of lupus and preclinical analysis suggest therapeutic activity for many other autoimmune diseases that share the same autophagy mechanism of action. ImmuPharma and Avion Pharmaceuticals signed on 28 November 2019, an exclusive licence and development agreement and trademark agreement for Lupuzor™ to fund a new international Phase 3 trial for Lupuzor™ and commercialise in the US.
For additional information about ImmuPharma please visit www.immupharma.co.uk
ImmuPharma's LEI (Legal Entity Identifier) code: 213800VZKGHXC7VUS895.
About Avion Pharmaceuticals LLC
Avion Pharmaceuticals, LLC, is a specialty pharmaceutical company formed to develop, acquire and market a portfolio of innovative pharmaceutical products in the Women's Health and other therapeutic categories aligned with its mission to improve the quality of patient lives. Avion Pharmaceuticals focuses on identifying opportunities to develop, acquire and enhance the market potential of innovative, commercially available therapeutics and late-stage development drugs to fulfil unmet medical needs. For more information, visit www.avionrx.com.
About Lupus (Systemic Lupus Erythematosus / SLE)
Lupus is a chronic inflammatory disease which is thought to affect some 5 million individuals worldwide. The current standard of care still consists of drugs which have many side-effects and limited efficacy. Despite the need for an effective treatment, only one new therapy, namely GlaxoSmithKline's Benlysta, has been approved to treat the condition over the past 50 years. As such, there clearly exists an unmet medical need for a drug that has a strong efficacy and safety profile.