Prescient Therapeutics

Company Announcements

Announcements

Unveiling of CellPryme-A adjuvant, designed to be administered to cancer patients to address the hostile tumour microenvironment that cellular immunotherapies face, thereby enhancing the ability of those therapies to kill cancer cells and improve host survival.
Click here to view the ASX announcement.

Strategic collaboration with MD Anderson Cancer Center, the largest cancer centre in the US, to develop unique blood cancer binders for OmniCAR. The agreement combines Prescient’s modular “plug and play” CAR platform with an undisclosed, proprietary binder discovered by MD Anderson’s ECLIPSE platform.
Click here to view the ASX announcement.

Like these videos? Click here to join our next investor briefing to learn more about Prescient Therapeutics

A production contract with Q-Gen, a specialist cell manufacturing company, to produce first OmniCAR T-cells for upcoming clinical trials, thereby helping Prescient progress towards its first in-human studies of OmniCAR – an important milestone for the company.
Click here to view the ASX announcement.

The US FDA granting ‘Orphan Drug Designation’ to Prescient’s PTX-100 for treating peripheral T-cell lymphomas – a disease with high unmet need. The benefits of an Orphan Drug Designation are considerable and include guaranteed market exclusivity of seven years from granting of regulatory approval.
Click here to view the ASX announcement. 

Live Investor Briefing

Prescient Therapeutics (ASX: PTX)

Tuesday, 4th October 12pm (AEDT)

Please join Prescient CEO and managing director Steven Yatomi-Clarke for an investor briefing.

In this session, Steven will discuss:

  • How PTX is taking the cancer treatment conversation from ‘fight’ to ‘cure’
  • How the company can potentially make any CAR-T developer’s therapies more effective, cheaper and safer
  • How its modular platform allows PTX to partner with any CAR-T developer giving them a ‘shovels to the gold rush’ position

It will be a fascinating look into why Prescient’s highly scalable business model gives them multiple shots on goal in oncology.

This is a live and interactive online session, and participants are encouraged to ask questions. Spots are limited, so secure yours today.

Attend the session

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Featured Speaker

 Michael Davidson

Steven Yatomi-Clarke

CEO and Managing Director

Steven took over as CEO of Prescient Therapeutics in 2016 and has overseen its progression from start-up phase. Steven manages a team in Australia and the US and has been instrumental in strategy development; licensing; initiating and managing clinical trials; fundraising and business development. He has been a collaborator on various immunotherapy research projects.

Dr Rebecca Lim

Dr Rebecca Lim

Senior Vice President of Scientific Affairs

Dr Rebecca Lim has over 10 years of experience in allogeneic cell therapies for regenerative medicine. She was previously the Scientific Director for the Cell Therapies Platform at the Hudson Institute and an Associate Professor at Monash University.

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What is a 708 investor?

By submitting this form, I agree to the terms of the Reach Markets Financial Services Guide that includes the Privacy Statement. Reach Markets has been engaged by Prescient Therapeutics Limited to assist with their investor communications and may receive fees for its services.

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Disclaimer and safe harbor

Certain statements made in this document are forward-looking statements within the meaning of the safe harbor provisions of the United States Private Securities Litigation Reform Act of 1995. These forward-looking statements are not historical facts but rather are based on the current expectations of Prescient Therapeutics Limited (“Prescient” or the “Company”), their estimates, assumptions, and projections about the industry in which Prescient operates. Material referred to in this document that use the words ‘estimate’, ‘project’, ‘intend’, ‘expect’, ‘plan’, ‘believe’, ‘guidance’, and similar expressions are intended to identify forward-looking statements and should be considered an at-risk statement. These forward-looking statements are not a guarantee of future performance and involve known and unknown risks and uncertainties, some of which are beyond the control of Prescient or which are difficult to predict, which could cause the actual results, performance, or achievements of Prescient to be materially different from those which may be expressed or implied by these statements. These statements are based on our management’s current expectations and are subject to a number of uncertainties and risks that could change the results described in the forward-looking statements. Risks and uncertainties include, but are not limited to, general industry conditions and competition, general economic factors, the impact of pharmaceutical industry development and health care legislation in the United States and internationally, and challenges inherent in new product development. Investors should be aware that there are no assurances that results will not differ from those projected and Prescient cautions shareholders and prospective shareholders not to place undue reliance on these forward-looking statements, which reflect the view of Prescient only as of the date of this presentation. Prescient is not under a duty to update any forward-looking statement as a result of new information, future events or otherwise, except as required by law or by any appropriate regulatory authority.


Certain statements contained in this document, including, without limitation, statements containing the words “believes,” “plans,” “expects,” “anticipates,” and words of similar import, constitute “forward-looking statements.” Such forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause the actual results, performance or achievements of Prescient to be materially different from any future results, performance or achievements expressed or implied by such forward-looking statements. Such factors include, among others, the following: the risk that our clinical trials will be delayed and not completed on a timely basis; the risk that the results from the clinical trials are not as favorable as we anticipate; the risk that our clinical trials will be more costly than anticipated; and the risk that applicable regulatory authorities may ask for additional data, information or studies to be completed or provided prior to their approval of our products. Given these uncertainties, undue reliance should not be placed on such forward-looking statements. The Company disclaims any obligation to update any such factors or to publicly announce the results of any revisions to any of the forward-looking statements contained herein to reflect future events or developments except as required by law.


This document may not contain all the details and information necessary for you to make a decision or evaluation. Neither this document nor any of its contents may be used for any other purpose without the prior written consent of the Company.


The contents of this document are confidential information of Prescient. These contents are made available on a ‘for your eyes only’ basis to the person to whom it was sent by Prescient. The purpose of the disclosure is to facilitate commercial and confidential discussions between the disclosee and Prescient. It should not be forwarded without the prior written consent of the Company.