Lupin and Yabao Announce Strategic Partnership in China

On April 27, 2022 Global pharma major Lupin Limited (Lupin) reported that it has entered into a strategic partnership with Yabao Pharmaceutical Co. Inc. (Yabao), to meet the growing demand for quality drugs with pediatric formulations in the Chinese markets (Press release, Lupin, APR 27, 2022, View Source [SID1234613252]).

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The demand for high quality pediatric medicines has been growing rapidly in China as a result of the government’s support and policy measures. The latest Chinese pediatric pharmaceutical market report indicates that the market for pediatric drugs in China is expected to reach 210 billion CNY (33 billion USD) in 2021, growing at a rate of 9.23%.

Dr. Fabrice Egros, President – Corporate Development and Growth Markets, Lupin said, "We are excited about this partnership as it paves the way for us to bring quality pediatric formulations to the growing needs of patients in China. In addition to marketing our pediatric products in the Chinese market, we intend to expand our collaboration in other strategic therapeutics areas such as cardio-metabolic, central nervous system and gastro-enterology."

Mr. Wei Ren, President of Yabao said, "We are very pleased to be partnering with Lupin to further strengthen Yabao’s leadership position in the pediatric market. Yabao strives to develop its pediatric pipeline to address the urgent unmet needs in the market and to serve the pediatric patients. Moreover, Yabao also looks forward to expanding the collaboration with Lupin in other areas."

United Therapeutics Corporation to Report First Quarter 2022 Financial Results Before the Market Opens on Wednesday, May 4, 2022

On April 27, 2022 United Therapeutics Corporation (Nasdaq: UTHR) reported that it will report its first quarter 2022 financial results before the market opens on Wednesday, May 4, 2022 (Press release, United Therapeutics, APR 27, 2022, View Source [SID1234613012]).

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United Therapeutics will host a public webcast Wednesday, May 4, 2022, at 9:00 a.m. Eastern Time. The webcast will be accessible via United Therapeutics’ website at View Source A rebroadcast of the webcast will be available for one week and can be accessed at the same location.

EXACT Therapeutics AS announces the publication of its 2021 Annual Report

On April 27, 2022 EXACT Therapeutics AS ("EXACT-Tx", Euronext Growth: EXTX), a clinical stage biopharmaceutical company with a mission to enhance the therapeutic efficacy of medicines through ultrasound-mediated drug delivery, reported that its Board of Directors has approved the Annual Report including the Annual Financial Statements for the year ended 31 December 2021 (Press release, Exact Therapeutics, APR 27, 2022, View Source [SID1234613031]).

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Zentalis Pharmaceuticals Announces $25 Million Equity Investment from Pfizer

On April 27, 2022 Zentalis Pharmaceuticals, Inc. (Nasdaq: ZNTL), a clinical-stage biopharmaceutical company focused on discovering and developing small molecule therapeutics targeting fundamental biological pathways of cancers, reported that it has agreed to sell 953,834 of its common shares at a price of $26.21 per share to Pfizer for gross proceeds of $25.0 million (the "Transaction") (Press release, Zentalis Pharmaceuticals, APR 27, 2022, View Source [SID1234613047]). The common shares were offered and sold to Pfizer in a registered direct offering conducted without an underwriter or placement agent. The offering is expected to close on or about April 29, 2022, subject to customary closing conditions. Zentalis intends to use the net proceeds of the offering to help fund ongoing and planned clinical trials, including studies of ZN-c3, its Wee1 inhibitor, and ZN-d5, its BCL-2 inhibitor, and for working capital and general corporate purposes. With prioritization of the clinical development of ZN-c3 and ZN-d5, budget reallocation and Pfizer’s investment, the Company extends current cash runway into Q1 2024.

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Pfizer also expects to leverage its global development capabilities and expertise to enhance Zentalis’ clinical development program. The parties have entered into an agreement to collaborate to advance the clinical development of ZN-c3, a selective Wee1 inhibitor designed to induce synthetic lethality in cancer cells.

Zentalis will maintain full economic ownership and control of ZN-c3 and the rest of its pipeline.

Dr. Anthony Sun, Chairman and Chief Executive Officer of Zentalis, commented, "Given Pfizer’s deep expertise in developing treatments for genitourinary cancers, we are proud not only to receive capital support but to partner with them to develop a potential treatment option for patients living with cancer. We look forward to advancing our promising therapeutics to hopefully realize the full potential of our internally discovered oncology pipeline."

"We are proud to support Zentalis and to assist in the clinical advancement of its pipeline," said Chris Boshoff, M.D., Ph.D., FMedSci, Chief Development Officer, Pfizer Oncology. "We believe Zentalis’ commitment to developing innovative treatments holds promise, and we are looking forward to continuing our relationship to potentially help better the lives of people with cancer."

In addition, Adam Schayowitz, Ph.D., MBA, Vice President & Medicine Team Group Lead for Breast Cancer, Colorectal Cancer and Melanoma, Pfizer, will join Zentalis’ Scientific Advisory Board. Dr. Schayowitz will work closely with Zentalis’ senior management team to provide input on the Company’s clinical strategy.

The securities described above were offered by means of a prospectus supplement dated April 26, 2022, and accompanying prospectus dated May 4, 2021, forming a part of the Company’s effective shelf registration statement (File No. 333-255769). The prospectus supplement and accompanying prospectus relating to this offering will be filed with the U.S. Securities and Exchange Commission (the "SEC") and will be available on the SEC’s website at www.sec.gov.

This press release shall not constitute an offer to sell or the solicitation of an offer to buy the common shares, nor shall there be any sale of the common shares in any state or other jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration or qualification under the securities laws of any such state or other jurisdiction.

Catamaran Bio Appoints Cherry Thomas, MD, as Chief Medical Officer

On April 27, 2022 Catamaran Bio, Inc., a biotechnology company developing off-the-shelf chimeric antigen receptor (CAR)-NK cell therapies to treat cancer, reported the appointment of Cherry Thomas, MD, as Chief Medical Officer (Press release, Catamaran Bio, APR 27, 2022, View Source [SID1234613064]). Dr. Thomas has broad experience in the clinical development of cell therapies. She initiated a first-in-human clinical trial of an allogeneic cell therapy during her previous role as senior vice president of clinical development at Caribou Biosciences. Dr. Thomas’ experience in oncology clinical development also includes leadership roles at Array BioPharma/Pfizer, Bristol Myers Squibb, Novartis, GlaxoSmithKline, and Amgen.

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"Cherry’s extensive experience in oncology and cell therapy drug development, clinical expertise, and impressive track record make her an ideal fit as we advance our innovative CAR-NK programs," said Alvin Shih, MD, Chief Executive Officer of Catamaran Bio. "We welcome Cherry at a pivotal time in our evolution, as we build the capabilities to become a clinical-stage company."

"I am excited to bring my clinical development experience with allogeneic cell therapies to a talented Catamaran team that has built a leading-edge platform for CAR-NK cell therapies," said Dr. Thomas. "I look forward to the opportunity to guide the clinical advancement of the Catamaran’s promising pipeline of allogeneic CAR-NK cell therapies, potentially becoming off-the-shelf treatments for patients with solid tumors."

Dr. Thomas has extensive pharmaceutical and biotech industry experience and expertise in the clinical development of oncology therapeutics including allogeneic cell therapies. Dr. Thomas joins Catamaran from Caribou Biosciences where she served as senior vice president of clinical development. In this role, she initiated and built Caribou’s clinical development program and advanced the company’s first allogeneic CAR-T cell therapy into the clinic. Prior to Caribou, she held positions of increasing responsibility and leadership in U.S. and global clinical development and medical affairs at Array BioPharma/Pfizer, Bristol Myers Squibb, Novartis, GlaxoSmithKline, and Amgen. Dr. Thomas received her MD from the University of California, Irvine, and completed her residency at the University of Michigan in radiation oncology and is a licensed physician and surgeon. She received her BA from the University of California, Los Angeles.