Onxeo Appoints Dr. Shefali Agarwal as President and Chief Executive Officer

On April 7, 2022 Onxeo S.A. (Euronext Growth Paris: ALONX, Nasdaq First North Copenhagen: ONXEO), hereafter "Onxeo" or the "Company", a clinical-stage biotechnology company specializing in the development of innovative drugs targeting tumor DNA Damage Response (DDR), reported the appointment of Dr. Shefali Agarwal as President and Chief Executive Officer (Press release, Onxeo, APR 7, 2022, View Source [SID1234611582]). Dr. Agarwal succeeds Julien Miara, a Principal at Invus SAS, who was named interim CEO in January 2022.

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"I have worked side by side with Dr. Agarwal in her capacity as Chairwoman to grow our Company, strengthen our Board and, importantly, advance our pipeline. It became very clear to me and the Board that Dr. Agarwal, who has extensive experience in drug development, was the right choice to fill the CEO role," said Julien Miara, interim CEO. "She has the expertise to partner with our strong team on expeditiously progressing AsiDNA through the clinic, developing our robust, pre-clinical pipeline and providing Onxeo with international visibility given her exposure among the U.S. investment community."

Dr. Agarwal is a physician by training, and, until recently, was the Chief Medical and Development Officer at Epizyme, Inc., a biopharmaceutical company developing novel epigenetic therapies for cancer, where she led global clinical development and regulatory strategy. She will remain an advisor to Epizyme in a consultant role while fulfilling her duties at Onxeo.

"I am honored to become the next CEO of Onxeo and look forward to working more closely with this talented team as we continue to grow the business. Given my deep experience in oncology, I’m encouraged by the work we’ve done at Onxeo and by the opportunities our platON platform has generated," said Dr. Shefali Agarwal. "As we continue to progress our first-in-class DDR inhibitor AsiDNA through the clinic and are conducting pre-clinical proof-of-concept studies on our next generation PARP agonist, OX401 and its followon optimized versions, we will be continually looking for ways to drive better clinical outcomes for patients. With an eye on the U.S. market, I’m pleased that we will be refocusing our clinical research efforts from France to the U.S., building out our infrastructure and expanding our team in the growing biotech hub in Massachusetts. The new influx of capital from our top two shareholders, who support our vision, will help us achieve our goals, providing Onxeo runway into Q2 2023."

Prior to joining Epizyme in 2018, Dr. Agarwal held various leadership positions across medical research, clinical development, clinical operations, and medical affairs. She served as chief medical officer at SQZ Biotech, where she built and led the clinical development organization, which included clinical research operations and the regulatory function. Before SQZ Biotech, she held leadership positions at Curis and Tesaro. At Curis, she oversaw the Phase 2 study for its dual HDAC/PI3K inhibitor in diffuse large B-cell lymphoma, and the Phase 1 study in solid tumors for its oral checkpoint inhibitor. At Tesaro, she led the NDA and EMA submissions for ZEJULA (niraparib) in ovarian cancer. Shefali has also held positions of increasing responsibility at Covidien, AVEO Oncology and Pfizer.

In addition to receiving her medical degree, Dr. Agarwal holds a Master of Public Health and a Master of Science in business. Dr. Agarwal is a member of the Board of Directors of three U.S. biotechnology companies, ITB Med (private), Gritstone Bio (NASDAQ: GRTS) and Fate Therapeutics (Nasdaq: FATE). She is also on the Scientific Advisory Board of Imvax, Inc. and is the Founder of Cancer Shakti Foundation, a voluntary non-profit organization dedicated to raising cancer awareness.

Robert L. Coleman, MD, Onxeo Board member and Chief Scientific Officer of US Oncology Research, said, "We are excited to welcome Dr. Agarwal to Onxeo as CEO. She brings unique expertise and clinical acumen to Onxeo, based on a successful history as a director in several biopharma companies. This bridging foundation provides a unique perspective into unmet clinical needs, treatment landscape, regulatory processes, and capital stewardship to carefully vet and execute on strategic initiatives for drug development and enterprise-level growth. I’m so honored to work alongside her to bring uniquely designed therapeutic assets to the clinic. On behalf of the Onxeo Board, we welcome Dr. Agarwal to her new leadership role."

OBI Pharma Announces Poster Presentations at AACR 2022 Annual Meeting for OBI-3424 and Globo H Science

On April 7, 2022 OBI Pharma, Inc. (TPEx: 4174) reported scientific data highlighting the antitumor synergy of OBI-3424 in combination with pembrolizumab (PD-1) and the association of high Globo H and PD-L1 expression resulting in poor survival in gastric cancer patients, will be presented at the American Association of Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting from April 8–13, 2022 in New Orleans, LA. (USA) (Press release, OBI Pharma, APR 7, 2022, View Source [SID1234611581]).

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OBI’s Chief Scientific Officer, Ming-Tain Lai, Ph. D stated that "OBI Pharma is proud to present at the AACR (Free AACR Whitepaper) Annual Meeting our latest scientific findings on the efficacy of OBI-3424 and the role of the Globo H antigen. OBI-3424 can induce immunogenic cell death and demonstrated impressive synergistic efficacy in combination with Pembrolizumab in various cancer models. Emerging science also demonstrated poor survival in gastric cancer patients who have high Globo H and PD-L1 expression. These findings warrant potential combination therapeutic strategies of OBI-3424 as well as anti-Globo H plus PD-1/PD-L1 cancer therapeutics ".

Title: OBI-3424, an AKR1C3-activated prodrug, exhibits in vivo synergistic anti-tumor effect in combination with pembrolizumab by induction of immunogenic cell death

Poster number: 6111 / Abstract number: 2922

Authors1 : Chun-Chung Wang, Wan-Fen Li, Chih-Chan Lee, Lu-Tzu Chen, Jhih-Jie Yang, Jiann-Shiun Lai, Ming-Tain Lai.

1OBI Pharma, Inc., Taipei, Taiwan.

Title: High Globo-H expression associated with poor survival of gastric cancer patients and enriched PD-L1 expression

Poster Number: 6138 / Abstract number: 1742

Authors: Tzer-Min Kuo1, Hui-Ting Hsu2,3, Cheng-Yen Wei1, Ming-Tain Lai1 and Chun-Te Chen1

1 OBI Pharma, Inc., Taipei, Taiwan.

2 Department of Pathology, Changhua Christian Hospital, Changhua, Taiwan.

3 Institute and School of Medicine, Chung Shan Medical University, Taichung, Taiwan.

The e-posters will be available for browsing at the AACR (Free AACR Whitepaper) Annual Meeting from 12:00 PM ET on April 8 and on the OBI Pharma website (www.obipharma.com) on April 9.

Lupin Completes Acquisition of Brands from Anglo-French

On April 7, 2022 Global pharma major Lupin Limited (Lupin) reported the completion of the acquisition of a portfolio of brands from Anglo-French Drugs & Industries Limited (AFDIL) and its Associates (Press release, Lupin, APR 7, 2022, View Source [SID1234611580]).

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The acquisition will strengthen Lupin’s India Formulation business by adding a fast-growing portfolio of vitamins, minerals, supplements and neurological products. The acquisition of the AFDIL brands takes Lupin further in shaping its portfolio to emerge as a leading pharmaceutical company in India.

"India is critical in shaping Lupin’s growth story going forward. This acquisition strengthens our position in the Indian market, where we have already established ourselves as a leading provider of quality pharmaceuticals and a trusted partner. With this portfolio, Lupin will have a stronger market presence, providing healthcare professionals and patients with a more meaningful and comprehensive product offering," said Nilesh Gupta, Managing Director, Lupin.

"The portfolio sold to Lupin was birthed by Anglo-French, and now, through this divestiture, we are confident that these brands will scale to a significant size and have a large impact on the health and well-being of the Indian population. We are confident in Lupin’s ability to enhance the value of our portfolio of brands," said Abhay Kanoria, Chairman & MD, AFDIL.

Shailesh Gadre, Founder of GCV Life was the exclusive advisor for the transaction.

Immunocore to present at the 21st Annual Needham Healthcare Conference

On April 7, 2022 Immunocore Holdings Plc (Nasdaq: IMCR), a commercial-stage biotechnology company pioneering the development of a novel class of T cell receptor (TCR) bispecific immunotherapies designed to treat a broad range of diseases, including cancer, infection and autoimmune disease, reported that management will participate in a fireside chat at the 21st Annual Needham Virtual Healthcare Conference (Press release, Immunocore, APR 7, 2022, View Source [SID1234611579]).

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The presentation is scheduled for Thursday, April 14, 2022 at 9:30 a.m. Eastern Time (ET).

The presentation will be webcast live during the conference and will be available in the ‘Investors’ section of Immunocore’s website at www.immunocore.com. A replay of the presentation will be made available for a limited time.

Celleron Therapeutics reports over 2-year survival of cancer patient treated with zabadinostat monotherapy

On April 7, 2022 Celleron Therapeutics, the UK-based company developing personalised medicines for cancer patients, reported a Phase I clinical trial cancer patient who continues to benefit from continuous zabadinostat therapy for over 2 years (Press release, Celleron, APR 7, 2022, View Source [SID1234611578]).

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CXD101-0901 is a clinical trial sponsored by Oxford University Hospitals NHS Foundation Trust, with support from Celleron Therapeutics. It is an open-label, Phase I study in patients with various advanced tumours where zabadinostat (formerly CXD101) is administered orally, twice daily, for 5 days, repeated every 3 weeks. The study began with a dose escalation phase to determine the maximum tolerated dose. Dose expansion was then opened at a recommended dose of 40mg daily. A total of 17 patients were treated in the dose expansion, which was closed to enrolment in 2019.

As of March 2022, one patient continues to receive zabadinostat monotherapy, having started treatment in December 2019. This patient has tolerated the drug well, experiencing few drug-related side effects with over 2 years of therapy. In terms of clinical response, the patient’s tumour has been effectively controlled during this extended period of time.

Dr Graham Collins, Principal Investigator and Haematology Consultant at the Oxford University Hospitals, commented:

"It’s really gratifying to have a patient with high-risk cancer responding so well for so long to an oral and well tolerated treatment."

Professor David Kerr, Chief Medical Officer of Celleron Therapeutics commented:

"We are excited by this encouraging long-term response to monotherapy, which adds to the continuing evidence that zabadinostat is a clinically viable drug with wide utility in clinically unmet disease. It is of interest that this subject has been able to tolerate dosing for more than 2 years, without experiencing any serious adverse drug reactions. We expect to further develop our understanding of this response with our upcoming large-scale clinical trials".