REACH: non-regulatory announcement
9
August 2024
Vela Technologies
plc
("Vela"
or "the Company")
Update re. investment in
Conduit Pharmaceuticals Inc.
The Board of Vela (AIM: VELA), an
AIM-quoted investing company focused on early stage and pre-IPO
disruptive technology investments, notes the announcement released
by Conduit Pharmaceuticals Inc. ("Conduit") on 8 August 2024 regarding
Conduit entering into an exclusive licence agreement with
AstraZeneca for multiple assets to advance potential first-in-class
treatments.
Vela holds 1,005,760 common shares
in Conduit representing 0.46% of Conduit's issued share capital. At
the closing mid-market price of $0.17 on 8 August 2024, Vela's
holding in Conduit is valued at approximately $170,000.
The full release from Conduit can be
accessed here (Conduit
Pharmaceuticals Enters into Exclusive License Agreement with
AstraZeneca for Multiple Assets to Advance Potential First-in-Class
Treatments | Nasdaq)
and is re-produced in full below.
For further information, please
contact:
Vela Technologies plc
Brent Fitzpatrick, Non-Executive
Chairman
James Normand, Executive
Director
|
Tel: +44 (0) 07950 389
469
|
Allenby Capital Limited (Nominated Adviser)
|
Tel: +44 (0) 20 3328 5656
|
Nick Athanas / Piers
Shimwell
|
|
Peterhouse Capital Limited (Broker)
|
Tel: +44 (0) 20 7469 0930
|
|
|
Novus Communications (PR and IR Adviser)
|
Tel: +44 (0) 20 7448 9839
|
Alan Green / Jacqueline
Briscoe
|
|
About Vela Technologies
Vela Technologies plc (AIM: VELA) is
an investing company focused on early stage and pre-IPO long term
disruptive technology investments. Vela's investee companies have
either developed ways of utilising technology or are developing
technology with a view to disrupting the businesses or sector in
which they operate. Vela Technologies will also invest in
already-listed companies where valuations offer additional
opportunities.
About Reach announcements
This is a Reach announcement. Reach
is an investor communication service aimed at assisting listed
and unlisted (including AIM quoted) companies
to distribute media only / non-regulatory news releases
into the public domain. Information required to be notified under
the AIM Rules for Companies, Market Abuse Regulation or other
regulation would be disseminated as an RNS regulatory announcement
and not on Reach.
Conduit Pharmaceuticals Enters into
Exclusive License Agreement with AstraZeneca for Multiple Assets to
Advance Potential First-in-Class Treatments
· Conduit Pharmaceuticals
enters into exclusive license agreement with AstraZeneca for HK-4
Glucokinase activators AZD1656 and AZD5658 targeting autoimmune
indications and myeloperoxidase inhibitor AZD5904 targeting
idiopathic male infertility
· Assets have shown favorable
preclinical and Phase I data. Conduit to initiate Phase II clinical
trials
SAN DIEGO and LONDON, Aug.
08, 2024 (GLOBE NEWSWIRE) --
Conduit Pharmaceuticals Inc.
(Nasdaq:
CDT) ("Conduit" or the
"Company"), today announced that the Company has entered into an
agreement with AstraZeneca to exclusively license rights to develop
AZD1656 and AZD5658, both HK-4 glucokinase activators, and AZD5904,
a myeloperoxidase inhibitor (MPO). AstraZeneca had progressed
AZD1656 and AZD5904 through Phase 1 clinical trials.
Conduit initially intends to conduct
Phase II clinical trials on clinical candidates AZD1656 and AZD5658
in 2024 for applications in autoimmune disorders, a category which
affect an estimated 10% of the population1.
Under the terms of the License
Agreement, AstraZeneca will grant Conduit an exclusive license to
both AZD1656 and AZD5658 for all human indications, as well as an
exclusive license to AZD5904 for use in Idiopathic Male
Infertility.
As part of the License Agreement,
AstraZeneca will be issued shares of common stock in Conduit, and
Conduit will also pay AstraZeneca a share of sublicense revenues,
including upfront payments, milestones, and royalties received from
future partners.
AstraZeneca will share pre-clinical
and clinical data on the assets and supply Conduit with certain
quantities of AZD1656, AZD5904, and AZD5658 from its inventory. The
License Agreement also includes provisions for the transfer of
know-how related to AZD1656, AZD5658 and AZD5904 from AstraZeneca
to Conduit. AstraZeneca has been granted a right of first
negotiation to develop, manufacture, and commercialize the licensed
compounds if Conduit seeks to assign, license, or grant such rights
to a third party.
Through the License Agreement,
Conduit will analyze existing clinical data and initiate Phase II
trials. Conduit believes this will fast-track the development of
these compounds and bring innovative new medicines to patients
facing substantial unmet needs.
"We are delighted to have entered
into an agreement with AstraZeneca to secure the rights to develop
AZD1656, AZD5658, and AZD5904. The potential of these assets to
become important first-in-class medicines for patients is
promising. Given the data from AstraZeneca's clinical trials, we
believe there is a strong rationale to initiate Phase II studies in
multiple indications to progress to commercialization of these
assets," said Dr. David Tapolczay, Chief
Executive Officer of Conduit.
Conduit departs from the traditional
business model of shepherding assets through an entire commercial
lifecycle by acquiring assets that have already undergone
pre-clinical and clinical testing. The Company works towards
accelerating the assets through Phase II trials and, if successful,
intends to seek exits through third-party license
opportunities.
About Conduit Pharmaceuticals
Conduit is a multi-asset, clinical
stage, disease-agnostic life science company delivering an
efficient model for compound development. Conduit both acquires and
funds the development of Phase II-ready assets and then seeks an
exit through third-party license deals following successful
clinical trials. Led by a highly experienced team of pharmaceutical
executives including Dr. David Tapolczay
and Dr. Freda Lewis-Hall, this novel
approach is a departure from the traditional pharma/biotech
business model of taking assets through regulatory
approval.