Trishula Therapeutics Established to Advance Novel TTX-030, an Anti-CD39 Antibody, Being Evaluated in Phase 1/1B Study in Advanced Cancers

On August 26, 2020 Trishula Therapeutics, a clinical stage, privately held company, reported that it was launched to be solely dedicated to the development of TTX-030, a first-in-class anti-CD39 antibody, being studied in advanced cancers (Press release, Trishula Therapeutics, AUG 26, 2020, View Source [SID1234572298]). The new company is designed to further progress and focus on the existing TTX-030 development collaboration with AbbVie.

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The Trishula launch is the result of the spin out of the TTX-030 program from Tizona Therapeutics with funds and employees to support its development. Shares in Trishula were distributed to Tizona shareholders, including MPM, Canaan, Abingworth, Lightstone, Interwest Partners, and AbbVie Ventures. Tizona’s current chief executive officer, Scott Clarke, will join the Trishula board and serve as its initial chief executive officer. Clarke will be joined by a seasoned team of experts focused on TTX-030, which is currently being studied in phase 1/1b clinical trials as a monotherapy and in combination with an anti-PD-1 agent and standard chemotherapy in adults with advanced cancer (NCT03884556 and NCT04306900).

"As a stand-alone company, Trishula will continue to deliver on the mission of bringing TTX-030, a novel, transformational medicine, to cancer patients in great need," said Scott Clarke, CEO, Trishula. "I have complete confidence that TTX-030 will continue to rapidly and effectively advance within Trishula and in partnership with AbbVie."

ChromaDex to Present at the LD 500 Virtual Investor Conference

On August 26, 2020 ChromaDex Corp. (NASDAQ:CDXC) reported that its Chief Executive Officer, Rob Fried , and Chief Financial Officer, Kevin Farr , will be presenting at the LD 500 investor conference (Press release, ChromaDex, AUG 26, 2020, View Source [SID1234568254]). The LD 500 will take place on September 1st through the 4th.

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The ChromaDex management team is scheduled to present on Wednesday, September 2, 2020 at 2:00 p.m. Eastern Time ( 11:00 a.m. Pacific Time ). The presentation will be webcast live via the link below on the investor relations section of the Company’s website at www.chromadex.com . ChromaDex management will also attend virtual one-on-one meetings with institutional investors throughout the day. For those interested in having a meeting with ChromaDex please contact David Scher at [email protected] or visit www.ldmicro.com for more information.

Prescient Therapeutics raises $7 million to fund cancer treatment pipeline

On August 26, 2020 Biotech Prescient Therapeutics (ASX: PTX) reported that it has successfully raised $7 million to fund an expanded pipeline of innovative cancer treatments (Press release, Prescient Therapeutics, AUG 26, 2020, View Source;utm_medium=rss&utm_campaign=prescient-therapeutics-raises-7-million-to-fund-cancer-treatment-pipeline [SID1234565484]).

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The clinical stage oncology company reported it has received firm commitments from professional and sophisticated investors for the placement of 128.1 million shares priced at $0.055 each to raise over $7 million before costs.

The placement immediately follows a recently completed oversubscribed $6.5 million share purchase plan, bringing the total funds raised to $13.5 million. Following settlement of the placement, Prescient confirmed it will have more than $20.3 million cash on hand.

Prescient chief executive officer and managing director Steven Yatomi-Clarke said the strong response for the placement partly reflected the excess demand for the share purchase plan.

"Both existing and new shareholders have shown that they share Prescient’s enthusiasm for its expanded pipeline of innovative cancer treatments," he said.

The placement shares are expected to be issued this Friday.

Use of funds
The company has assigned some of the funds for the development of targeted therapies and cell therapy enhancement programs.

"These funds will also be applied towards the development of OmniCAR, a next generation CAR-T platform that aims to significantly broaden CAR-T’s addressable market, while overcoming many limitations of existing CAR-T therapies," Mr Yatomi-Clarke said.

"These represent tremendous market opportunities. We welcome new shareholders as they join us on our journey to develop innovative and personalised cancer therapies," he added.

The placement funds will also be used for working capital and to pay the costs of the offer.

CAR-T technology
CAR-T technology is a type of cellular therapy that reprograms a cancer patient’s immune cells to recognise and destroy cancer.

Mr Yatomi-Clarke joined Small Caps last week in a podcast talking about Prescient’s next-generation CAR-T platform, OmniCAR.

"For the very first time, thanks to this brand new approach (CAR-T therapy) we’re seeing responses that we’ve not yet seen in cancer before that are akin to cures…Some are calling it the beginning of the end which is incredibly exciting to contemplate," he said.

"The problem with cancer is that it’s mutated at surface just enough to avoid surveillance from the immune system, so the T-cells – the frontline soldiers of the immune system – don’t recognise the cancer anymore."

Mr Yatomi-Clarke said Prescient’s technology modifies and trains the receptor of the T-cells in a patient’s own immune system so they can detect cancer again.

"We are seeing unparalleled cancer-killing capabilities with this type of therapy that has caused durable remissions in patients that have failed everything else… it’s a remarkably exciting new frontier of cancer [treatment] that we’re in," he said.

Targeted therapies
Prescient’s other approach to cancer is targeted therapies and it is developing two drug candidates, PTX-100 and PTX-200.

Mr Yatomi-Clarke described targeted therapies as injectable medicines that "finds the mutations or drivers of the cancer and switches them off – so the things that make it divide in an uncontrolled manner".

PTX-100 is currently in a pharmacokinetics/pharmacodynamics (PK/PD) basket study of hematological and solid malignancies, focusing on cancers with Ras and RhoA gene mutations. It is believed to be the only RhoA inhibitor in the world in clinical development, according to Prescient.

PTX-200 is a novel PH domain inhibitor that inhibits the Akt tumour survival pathway, which plays a role in the development of breast and ovarian cancers, as well as leukemia. It achieved encouraging results from a Phase 2a study on HER2-negative breast cancer, Phase 1b/2 in relapsed and refractory acute myeloid leukemia and Phase 1b in recurrent or persistent platinum resistant ovarian cancer.

Prescient also recently announced two of its assets are being assessed by the Doherty Institute in Melbourne for antiviral activity against SARS-CoV-2, the virus that causes COVID-19.

Phosplatin Therapeutics Completes $18.4 Million Private Financing Round

On August 26, 2020 Phosplatin Therapeutics LLC, a clinical stage pharmaceutical company focused on oncology therapeutics, reported the completion of an oversubscribed $18.4 million private financing round (Press release, Phosplatin, AUG 26, 2020, View Source [SID1234564995]). Participation included new and existing investors, inclusive of family offices from the US, Europe and Asia-Pacific, and high net worth individuals.

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Robert Fallon, President and Chief Executive Officer of Phosplatin Therapeutics, commented, "The success of the financing underscores the breadth of our data from three different Phase I trials and the broad potential of our lead compound, PT-112, which is advancing through clinical development as a monotherapy, including in mCRPC and multiple myeloma, and in combination with PD-L1 immune checkpoint inhibition. We plan to utilize the proceeds of this capital raise to complete Phase 2 development of PT-112, and our continued planning prior to launching intended pivotal trials."

Phosplatin Therapeutics has raised $56 million in equity capital since inception, and receives milestone fees from its sub-licensee for Greater China.

About PT-112

PT-112 is the first small molecule conjugate of pyrophosphate developed in oncology therapeutics. PT-112 promotes immunogenic cell death (ICD), or the release of damage associated molecular patterns (DAMPs) that lead to downstream immune effector cell recruitment in the tumor microenvironment. PT-112 represents a potential best-in-class small molecule inducer of this immunological form of cancer cell death, and is under Phase 2 development. The first-in-human study of PT-112 demonstrated an attractive safety profile and evidence of long-lasting responses among heavily pre-treated patients, and won "Best Poster" at the ESMO (Free ESMO Whitepaper) 2018 Annual Congress within the Developmental Therapeutics category. The novelty of its pyrophosphate moiety also results in osteotropism, or the propensity of the drug to reach the mineralized bone. This property is of interest in cancer types that originate in bone, or frequently lead to metastatic bone involvement, such as metastatic castrate-resistant prostate cancer (mCRPC). The first human clinical results in mCRPC were presented at the 2020 Genitourinary Cancers Symposium.

New FDA Approval for FoundationOne Liquid CDx Biomarker Testing

On August 26th, 2020, Bonnie J Addario Lung Cancer Foundation reported that the Food and Drug Administration (FDA) approved the FoundationOne Liquid CDx for comprehensive liquid biopsy biomarker testing for patients with any solid tumor (Press release, Bonnie J Addario Lung Cancer Foundation, AUG 26, 2020, View Source [SID1234564229]). The FDA based their approval on analysis from multiple clinical validation studies which showed that FoundationOne Liquid CDx is very sensitive and specific in finding mutations.

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This approval gives patients more options for comprehensive liquid biopsy biomarker testing that were not previously available.