Immupharma PLC FDA response for Type C Meeting - update (6692X)
31 Agosto 2022 - 8:01AM
UK Regulatory
TIDMIMM
RNS Number : 6692X
Immupharma PLC
31 August 2022
31 August 2022
ImmuPharma plc
("ImmuPharma" or the "Company")
FDA response for Type C Meeting - update
ImmuPharma plc (LSE : IMM), the specialist drug discovery and
development company, announced on 7 July 2022 that its US partner
for Lupuzor(TM) (P140), Avion Pharmaceuticals ("Avion"), had
advised that it had received Type C Meeting confirmation from the
Food and Drug Administration ("FDA").
It was announced at that time that : the statement of purpose,
objectives, and proposed agenda of the Type C meeting have been
agreed with the FDA, that the FDA also agreed that written
responses to the agenda items would be the most appropriate means
for responding and that a face to face meeting was not required,
and that the agreed date from the FDA for providing its written
responses was 29 August 2022.
As of 30 August 2022, Avion has not yet received the written
response from the FDA. The Company is in close contact with Avion
and have been advised that the FDA is experiencing general delays
in meeting response dates and that this is not specific to Avion
and the Type C meeting for Lupuzor(TM) (P140). The Company will
notify the market as soon as practicable once a response from the
FDA has been received.
This announcement contains inside information for the purposes
of Article 7 of EU Regulation 596/2014.
For further information please contact:
ImmuPharma PLC ( www.immupharma.com )
Tim McCarthy, Chairman + 44 (0) 207 152 4080
Lisa Baderoon, Head of Investor Relations + 44 (0) 7721 413496
SPARK Advisory Partners Limited (NOMAD)
Neil Baldwin
Stanford Capital Partners (Joint Broker) +44 (0) 203 36 8 3550
Patrick Claridge
John Howes
Bob Pountney +44 (0) 203 815 8880
SI Capital (Joint Broker)
Nick Emerson +44 (0) 1483 413500
Notes to Editors
About ImmuPharma PLC
ImmuPharma PLC (LSE AIM: IMM) is a specialty biopharmaceutical
company that discovers and develops peptide-based therapeutics. The
Company's portfolio includes novel peptide therapeutics for
autoimmune diseases and anti-infectives. The lead program,
Lupuzor(TM), 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
Alora Pharmaceuticals signed on 28 November 2019, an exclusive
licence and development agreement and trademark agreement for
Lupuzor(TM) to fund a new international Phase 3 trial for
Lupuzor(TM) and commercialise in the US.
For additional information about ImmuPharma please visit
www.immupharma.com. ImmuPharma's LEI (Legal Entity Identifier)
code: 213800VZKGHXC7VUS895.
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END
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