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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 Ast

Key Takeaway: Conduit Pharmaceuticals has entered into an exclusive license agreement with AstraZeneca for three promising assets, including HK-4 glucokinase activators and a myeloperoxidase inhibitor. These compounds are poised for development targeting autoimmune disorders and idiopathic male infertility, with Phase II trials expected to commence in 2024. AstraZeneca will provide support through data sharing and inventory supplies. This strategic move highlights Conduit's novel approach to accelerating drug development via licensing established assets.

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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
DIEGO and LONDON, August 8, 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.
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.
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.
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.
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.
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.
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."
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.
Conduit Pharmaceuticals
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.
press release contains certain forward-looking statements within the meaning of the federal securities laws. All statements other than
statements of historical facts contained in this press release, including statements regarding Conduit's future results of operations
and financial position, Conduit's business strategy, prospective product candidates, product approvals, research and development
costs, timing and likelihood of success, plans and objectives of management for future operations, future results of current and anticipated
studies and business endeavors with third parties, and future results of current and anticipated product candidates, are forward-looking
statements. These forward-looking statements generally are identified by the words "believe," "project," "expect,"
"anticipate," "estimate," "intend," "strategy," "future," "opportunity,"
"plan," "may," "should," "will," "would," "will be," "will
continue," "will likely result," and similar expressions. These forward-looking statements are subject to a number
of risks, uncertainties and assumptions, including, but not limited to; the inability to maintain the listing of Conduit's securities
on Nasdaq; the ability to recognize the anticipated benefits of the business combination completed in September 2023, which may be affected
by, among other things, competition; the ability of the combined company to grow and manage growth economically and hire and retain key
employees; the risks that Conduit's product candidates in development fail clinical trials or are not approved by the U.S. Food
and Drug Administration or other applicable authorities on a timely basis or at all; changes in applicable laws or regulations; the possibility
that Conduit may be adversely affected by other economic, business, and/or competitive factors; and other risks as identified in filings
made by Conduit with the U.S. Securities and Exchange Commission. Moreover, Conduit operates in a very competitive and rapidly changing
environment. Because forward-looking statements are inherently subject to risks and uncertainties, some of which cannot be predicted
or quantified and some of which are beyond Conduit's control, you should not rely on these forward-looking statements as predictions
of future events. Forward-looking statements speak only as of the date they are made. Readers are cautioned not to put undue reliance
on forward-looking statements, and except as required by law, Conduit assumes no obligation and does not intend to update or revise these
forward-looking statements, whether as a result of new information, future events, or otherwise. Conduit gives no assurance that it will
achieve its expectations.
Pharmaceuticals Inc.

Frequently Asked Questions

What is the agreement between Conduit and AstraZeneca?

Conduit Pharmaceuticals has signed an exclusive license agreement with AstraZeneca for drug development.

What treatments are being developed under this agreement?

The agreement covers HK-4 glucokinase activators AZD1656 and AZD5658, and AZD5904.

What stage are the clinical trials for these assets?

Conduit plans to start Phase II clinical trials for these assets in 2024.

What conditions do the licensed drugs target?

The licensed drugs target autoimmune disorders and idiopathic male infertility.

How does Conduit's business model differ from traditional pharma?

Conduit focuses on accelerating already tested assets through Phase II trials rather than developing from scratch.

Last updated: Aug 8, 2024