Lilly to Participate in Guggenheim Oncology Conference

On February 1, 2022 Eli Lilly and Company (NYSE: LLY) reported that it will participate in the Guggenheim Oncology Conference on Wednesday, Feb. 9, 2022 (Press release, Eli Lilly, FEB 1, 2022, View Source [SID1234607564]). Jake Van Naarden, CEO of Loxo Oncology at Lilly and president, Lilly Oncology and David Hyman, M.D., chief medical officer, Lilly Oncology, will participate in a virtual fireside chat at 12 p.m., Eastern time .

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A live audio webcast will be available on the "Webcasts & Presentations" section of Lilly’s Investor website at View Source A replay of the presentation will be available on this same website for approximately 90 days.

Eagle Pharmaceuticals Announces Commercial Availability of PEMFEXY™

On February 1, 2022 Eagle Pharmaceuticals, Inc. (Nasdaq: EGRX) ("Eagle" or the "Company") reported the commercial availability of its novel product PEMFEXY (pemetrexed for injection) (Press release, Eagle Pharmaceuticals, FEB 1, 2022, View Source [SID1234607563]). A branded alternative to ALIMTA, Eagle’s PEMFEXY is a ready-to-use liquid with a unique J-code approved to treat nonsquamous non-small cell lung cancer and mesothelioma.

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"We’ve spent the past several months building our inventory and are pleased that PEMFEXY will now be available to the many patients who need it. Together with our recent launch of vasopressin and now PEMFEXY, these products represent significant opportunities for Eagle," stated Scott Tarriff, President and Chief Executive Officer.

In February 2020, Eagle received final approval from the U.S. Food and Drug Administration of its New Drug Application for PEMFEXY, following the settlement agreement of patent litigation with Eli Lilly and Company (NYSE: LLY) in December 2019. The agreement provided for a release of all claims by the parties and allows for an initial entry of PEMFEXY into the market (equivalent to approximately a three-week supply of current ALIMTA utilization) on February 1, 2022 and a subsequent uncapped entry on April 1, 2022.

On October 1, 2020, PEMFEXY’s Healthcare Common Procedure Coding System code, or J-code, became effective.

About PEMFEXY

PEMFEXY is a pemetrexed injection ready-to-dilute formulation for locally advanced or metastatic nonsquamous non-small cell lung cancer in combination with cisplatin; locally advanced or metastatic nonsquamous non-small cell lung cancer whose disease has not progressed after four cycles of platinum-based first-line chemotherapy, as maintenance treatment; locally advanced or metastatic nonsquamous non-small cell lung cancer after prior chemotherapy as a single agent; and malignant pleural mesothelioma whose disease is unresectable or who are otherwise not candidates for curative surgery in combination with cisplatin.

Akhil Ravi appointed CEO of Aurigene Pharmaceutical Services Ltd.

On February 1, 2022 Dr. Reddy’s Laboratories Ltd. along with its subsidiaries together referred to as "Dr. Reddy’s") reported that it named Akhil Ravi as CEO for its wholly-owned subsidiary Aurigene Pharmaceutical Services Ltd. (APSL) effective February 1, 2022 (Press release, Dr Reddy’s, FEB 1, 2022, View Source [SID1234607562]).

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Since joining Dr. Reddy’s in 2018 from McKinsey & Company, Akhil Ravi has served as Head of Strategy for Services and Active Pharmaceutical Ingredients (APIs), and headed the Sales of APIs in Europe. In addition, he has also had a brief stint as Plant Head. Akhil holds a BTech degree in Chemical Engineering from IIT Bombay and an MBA from the Indian School of Business (ISB).

"Akhil is very well prepared for this role. He was instrumental in growing our API business through product development and an improved service experience for our B2B customers through digital platforms. His strong background in customer service, sales, strategy, and management make him an ideal leader for Aurigene, and we look forward to his accomplishments in this new role." said Deepak Sapra, CEO of API and Services at Dr. Reddy’s, and Member of the Board at Aurigene.

Akhil Ravi said: "Aurigene Pharmaceutical Services is a dynamic partner for global pharma companies. With its integrated services from clinical research up to commercial manufacturing for small and large molecules, it is able to significantly speed up the journey of an NCE/NBE (New Chemical and Biological Entities) to the patient. I am very thrilled to join Aurigene and work with the team to serve innovative global pharma and biotech companies."

Deciphera Pharmaceuticals to Announce Fourth Quarter and Full Year 2021 Financial Results and Host Conference Call and Webcast on February 8, 2022

On February 1, 2022 Deciphera Pharmaceuticals, Inc. (NASDAQ: DCPH) reported that it will report its fourth quarter and full year 2021 financial results on Tuesday, February 8, 2022 (Press release, Deciphera Pharmaceuticals, FEB 1, 2022, View Source [SID1234607560]).

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In connection with the earnings release, Deciphera’s management team will host a live conference call and webcast at 4:30 PM ET on Tuesday, February 8, 2022, to discuss the Company’s financial results and provide a corporate update.

The conference call may be accessed by dialing (866) 930-5479 (domestic) or (409) 216-0603 (international) and referring to conference ID 8293127. A webcast of the conference call will be available in the "Events and Presentations" page in the "Investors" section of the Company’s website at View Source The archived webcast will be available on the Company’s website approximately two hours after the conference call and will be available for 30 days following the call.

Biomea Fusion Announces Appointment of Steve Morris, M.D. as Chief Medical Officer

On February 1, 2022 Biomea Fusion, Inc. ("Biomea") (Nasdaq: BMEA), a clinical-stage biopharmaceutical company dedicated to the discovery and development of novel irreversible small molecules to treat and improve the lives of patients with genetically defined cancers and metabolic diseases, reported the appointment of Steve Morris, M.D. as Chief Medical Officer (CMO) (Press release, Biomea Fusion, FEB 1, 2022, View Source [SID1234607558]). Dr. Morris, who has been serving as a clinical consultant to Biomea since 2020, will now lead the clinical development of BMF-219, an irreversible covalent menin inhibitor, as well as the company’s additional planned clinical programs. BMF-219 is currently in a Phase I clinical trial for the treatment of patients with relapsed/refractory acute leukemias, including those with MLL1/KMT2A gene rearrangements or NPM1 mutations. In January 2022, Biomea announced that it plans to initiate clinical studies of BMF-219 in up to seven liquid and solid tumor types –acute myeloid leukemia (AML) and acute lymphocytic leukemia (ALL), multiple myeloma (MM), diffuse large B-cell lymphoma (DLBCL), non-small cell lung cancer (NSCLC), pancreatic cancer, and colorectal cancer– as well as diabetes.

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"I am thrilled with Steve’s decision to join Biomea full-time as the company’s first CMO," said Thomas Butler, Biomea’s CEO and Chairman of the Board. "Steve is an internationally recognized physician-scientist and translational investigator with over 30 years of clinical and academic research expertise. Through his first-hand experience interrogating the role that menin plays in aggressive cancers both as a researcher and as a practicing oncologist, Steve has a unique perspective on how BMF-219 may benefit patients suffering from genetically driven liquid and solid tumors. He played a critical role in orchestrating our rapid advancement of BMF-219 into the clinic, and we look forward to his continued contributions in this new capacity as our CMO."

Prior to embarking on a career in the biopharmaceutical industry in 2012, Dr. Morris served on the staff at St. Jude Children’s Research Hospital for 25 years. In addition to working as a clinician, he led a basic and translational research laboratory at St. Jude, which discovered and characterized oncogenes that cause a variety of human cancers, most notably anaplastic lymphoma kinase, or ALK. The U.S. Food and Drug Administration (FDA) has approved several ALK inhibitors, the development of which were based on Dr. Morris’ groundbreaking work. Dr. Morris also performed translational research at St. Jude regarding menin-driven leukemias (one of several menin-driven oncology indications being pursued by Biomea) and treated many patients with these malignancies during his career as a practicing oncologist.

"I am excited to continue the extraordinary work we have done at Biomea over the last two years translating the promise of Biomea’s Fusion platform, which allows the rapid targeting of validated cancer biology with breakthrough covalent chemistry, to advance the company’s first clinical-stage irreversible covalent inhibitor, BMF-219," said Dr. Morris. "With the potential to dose patients in up to seven distinct tumor types with BMF-219 in the coming months, 2022 will be a transformational year for Biomea. I look forward to continuing to execute on the robust clinical development plan we announced to further our collective goal of providing effective targeted treatments for patients with limited therapeutic options."

Since leaving academic medicine, Dr. Morris has served as a consultant or CMO for multiple oncology-focused biotech startups, including Biomea. He is a member of the medical honor society Alpha Omega Alpha, an American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Young Investigator Award winner, and an inductee into the American Society for Clinical Investigation. Dr. Morris earned his MD from Louisiana State University Health Science Center, completed an internal medicine residency at the University of Texas Southwestern Health Science Center, and completed training in medical oncology at Yale University School of Medicine.