RNS
REACH
TheraCryf
plc
("TheraCryf", the "Company" or the "Group")
Publication of peer reviewed
data on healthy volunteer pharmacokinetic study
of SFX-01 novel tablet in Advances in Therapy
Alderley Park, UK - 11 November 2024: TheraCryf
plc (AIM: TCF), the clinical stage drug
development company focussing on oncology and
neuropsychiatry announces publication
of the pharmacokinetic and safety/tolerability data on
lead clinical asset SFX-01 from its Ph1b healthy volunteer study in
the peer reviewed journal, Advances in Therapy.
The publication, which can be found here,
reports on the findings of the study which aimed to investigate how
the new SFX-01 enteric-coated tablet formulation performed and how
sulforaphane released from the novel formulation was metabolised in
the bloodstream of the healthy volunteers and subsequently
excreted.
As announced previously in August 2023, the
data from the study demonstrated that the Company's new enteric
coated tablet formation of lead asset SFX-01 was shown to perform
as designed, delivering drug and active metabolites, as well as
being safe and well tolerated.
The publication concluded that the data from
the phase 1 randomized, double-blinded, placebo-controlled,
dose-escalation study demonstrated:
·
SFX-01 was well tolerated over 7 days at the doses evaluated,
with most side-effects being mild and transient in
nature.
· The
pharmacokinetic properties of the SFX-01 tablet formulation were in
line with expectations, suggesting that enteric coating and
stabilization of sulforaphane delivers levels of SFN and
metabolites in the range where biological activity is
observed.
This publication was authored by TheraCryf's
Chief Medical Officer, Dr Glen Clack, and Vice-President, Project
Management, Dr Nicholas Mallard, along with consultants to the
Company.
Dr Helen
Kuhlman, TheraCryf's CBO, commented:
"We are
pleased to see our data published in a peer reviewed academic
journal. Our study is a definitive examination of sulforaphane's
pharmacokinetics from our proprietary enteric coated tablet and
provides a detailed analysis of the delivery and handling of
sulforaphane from SFX-01 tablets by the body."
Dr Glen Clack,
TheraCryf's CMO added:
"These data
prepare us well for future studies, in particular glioblastoma
patients in our grant funded collaboration with the Erasmus Medical
Centre Rotterdam, NL."
-Ends-
Enquiries
TheraCryf plc
Dr Huw Jones, CEO
Toni Hänninen, CFO
Dr Helen Kuhlman, CBO
|
+44 (0)1625 315
090
enquiries@theracryf.com
|
Cavendish Capital Markets (NOMAD and Broker)
Geoff Nash / Teddy Whiley / Rory Sale (Corporate
Finance)
Nigel Birks / Harriet Ward
(ECM)
|
+44 (0)20
7220 0500
|
Vigo Consulting Rozi
Morris
|
+44 (0)20 7390 0231
theracryf@vigoconsulting.com
|
About TheraCryf plc
TheraCryf is the clinical stage drug
development company focussing on oncology and neuropsychiatry. The
Company has a broad clinical and preclinical pipeline in
indications including glioblastoma* neurodevelopmental disorders,
addiction, anxiety and narcolepsy [*orphan indication].
The Company's strategy is to
generate compelling data sets to preclinical and/or clinical proof
of concept and partner its clinical programmes with mid-size to
large pharma for larger trials and commercialisation. As well as a
number of industry partnerships with companies, including Stalicla
SA, in neurodevelopmental disorders. The Company has sourced
know how for programmes from companies such as Shire (now
Takeda).
TheraCryf has worked with and has
ongoing collaborations with major universities and hospitals such
as the University of Manchester, La Sapienza (Università di Roma),
the Erasmus Medical Centre, Rotterdam, Kings College London and the
University of Michigan.
The Company has its headquarters and
registered office at Alderley Park, Cheshire. It is quoted on AIM
in London and trades under the ticker symbol TCF.
For further information, please
visit: www.theracryf.com