Alexion to Present at the 2019 Evercore ISI HealthCONx

On November 26, 2019 Alexion Pharmaceuticals (Nasdaq:ALXN) reported that management will present at the 2019 Evercore ISI HealthCONx in Boston, MA on Tuesday, December 3rd, 2019 at 8:45 a.m. ET (Press release, Alexion, NOV 26, 2019, https://news.alexionpharma.com/press-release/financial-news/alexion-present-2019-evercore-isi-healthconx [SID1234551694]).

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An audio webcast of the presentation will be available live. You can access the webcast at: View Source An archived version of the remarks will also be available through the Company’s website for a limited time following the conference.

BIO-PATH HOLDINGS ANNOUNCES SUCCESSFUL COMPLETION OF SAFETY TESTING IN STAGE 2 OF PHASE 2 CLINICAL TRIAL IN ACUTE MYELOID LEUKEMIA

On November 26, 2019 Bio-Path Holdings, Inc., (NASDAQ:BPTH), a biotechnology company leveraging its proprietary DNAbilize antisense RNAi nanoparticle technology to develop a portfolio of targeted nucleic acid cancer drugs, reported the successful completion of the safety testing of prexigebersen in combination with decitabine in acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS) patients in Stage 2 of the Phase 2 clinical study (Press release, Bio-Path Holdings, NOV 26, 2019, View Source [SID1234551689]). The safety segment of Stage 2 of the Phase 2 clinical trial comprised six evaluable patients who were treated with the combination of prexigebersen and decitabine.

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"We are especially pleased to have successfully completed this key safety segment of our Phase 2 study as it allows us to move forward to the next segment of this important clinical study, which is the final, efficacy portion of Stage 2 of the Phase 2 study," said Peter Nielsen, President and Chief Executive Officer of Bio-Path Holdings. "We are in the process of completing the documentation to submit for final approval of this last portion of Stage 2 of the Phase 2 study. These results are encouraging and give us greater confidence in the successful development of this very promising combination therapy for AML and MDS patients."

Although the treatment combination of prexigebersen and decitabine is not the treatment planned for the efficacy evaluation of Stage 2 of the Phase 2 clinical trial, the efficacy profile in this safety segment of the study was encouraging with 50% of patients having a response, including two patients (33%) showing complete responses with incomplete hematologic recovery and one patient (17%) showing partial response. For reference, in this class of AML and MDS patients, the complete response rate to treatment with decitabine alone is approximately 20%. Some patients are continuing to receive treatment.

As previously reported, Stage 1 of the Phase 2 clinical trial, which treated de novo AML patients with a combination of low dose cytarabine (LDAC) and prexigebersen, demonstrated similar safety results and efficacy compared favorably to treatment of this class of patients with LDAC alone. We believe that prexigebersen with its promising efficacy and safety profile, has the potential to be an ideal combination candidate with frontline therapy. The recent approval of the frontline therapy venetoclax provided an opportunity for adding prexigebersen to the combination of venetoclax and decitabine for the treatment of AML and MDS patients. The first step in this process was establishing the safety of combining prexigebersen and decitabine prior to proceeding to a combination treatment of prexigebersen, decitabine and venetoclax.

Bio-Path’s amended Stage 2 of the Phase 2 clinical trial will have two cohorts of patients. The first cohort will include untreated AML patients as existed in the pre-amended trial but with the addition of untreated high risk MDS patients, and a second cohort will include refractory/relapsed AML patients and high risk MDS patients. Both cohorts of patients will be treated with the combination of prexigebersen, decitabine and venetoclax. The Company is finalizing amendments to add this combination treatment to Stage 2 of the Phase 2 clinical trial.

Curis to Present at 31st Annual Piper Jaffray Healthcare Conference

On November 26, 2019 Curis, Inc. (NASDAQ: CRIS), a biotechnology company focused on the development of innovative therapeutics for the treatment of cancer, reported that James Dentzer, Chief Executive Officer of Curis, will present at the 31st Annual Piper Jaffray Healthcare Conference on Tuesday, December 3, 2019 at 11:30 a.m. ET in New York, NY (Press release, Curis, NOV 26, 2019, View Source [SID1234551688]).

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A live webcast of the presentation will be available under "Events & Presentations" in the Investors section of the Company’s website at www.curis.com. A replay of the webcast will be available on the Curis website for 90 days following the event.

Sutro Biopharma to Participate in the 31st Annual Piper Jaffray Healthcare Conference

On November 26, 2019 Sutro Biopharma, Inc. (NASDAQ: STRO), a clinical-stage drug discovery, development and manufacturing company focused on the application of precise protein engineering and rational design to create next-generation oncology therapeutics, reported that it will present at the 31st Annual Piper Jaffray Healthcare Conference on Tuesday, Dec. 3, 2019, at 4 p.m. EST in New York (Press release, Sutro Biopharma, NOV 26, 2019, View Source [SID1234551687]).

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A live webcast of the presentation will be accessible through the Events and Presentations page of the Investor Relations section of the company’s website at www.sutrobio.com. A replay of the webcast will be available for approximately 30 days following the event.

Sierra Oncology Announces Closing of $103 Million Public Offering and Changes to its Board of Directors

On November 26, 2019 Sierra Oncology, Inc. (Nasdaq: SRRA), a late-stage drug development company focused on the development and commercialization of momelotinib, a JAK1, JAK2 & ACVR1 inhibitor with a potentially differentiated therapeutic profile for the treatment of myelofibrosis, reported that it has closed its previously announced underwritten public offering, with gross proceeds to Sierra Oncology of $103 million (Press release, Sierra Oncology, NOV 26, 2019, View Source [SID1234551686]).

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Following the closing of this offering, Mr. Robert Pelzer, who has served as a member of the company’s Board of Directors since May 2015, has been appointed as the Chairman of the Board of Directors. Sierra Oncology has also appointed Dr. Gaurav Aggarwal, Dr. Josh Richardson, Dr. Mona Ashiya and Dr. Andrew Sinclair to the Board of Directors, each of whom are affiliated with investors in the offering. In addition, Mr. Donald Parfet, Dr. Daniel Estes, Dr. Nicole Onetto and Mr. Tran Nguyen have resigned from the Board of Directors. The foregoing appointments and resignations were effective as of November 22, 2019.

"It is a pleasure to welcome these outstanding individuals to our Board of Directors. Their support and guidance will be invaluable as we focus on executing the recently launched MOMENTUM Phase 3 trial of momelotinib and prepare the groundwork for our potential transition to a commercial entity," said Mr. Robert Pelzer. "We would also like to sincerely thank our outgoing members for their service and dedication to the company. In particular, we are extremely grateful to Don Parfet, who has served as Chairman of our Board of Directors since the company’s inception in 2003, for his thoughtful leadership and unwavering dedication to Sierra Oncology."

Robert Pelzer has served as a member of our Board of Directors since May 2015. From September 2008 to March 2013, Mr. Pelzer served as the President of Novartis Corporation, a pharmaceutical company. From 2002 to 2008, Mr. Pelzer served as General Counsel at Novartis Pharma AG. Prior to 2002, Mr. Pelzer held various positions, including serving as General Counsel and Senior Vice President at DuPont Pharmaceuticals from 1998 to 2001. Mr. Pelzer currently serves on the Board of Directors of Qu Biologics and previously served on the Board of Directors of Aquinox Pharmaceuticals and Idenix Pharmaceuticals, Inc. Mr. Pelzer holds a BComm and an LL.B. from the University of Alberta.

Gaurav Aggarwal, M.D., has served as a Managing Director of Vivo Capital LLC, a healthcare focused investment firm, since October 2016, where he focuses on investments in life sciences companies. Dr. Aggarwal previously served as the Chief Business Officer of Ocera Therapeutics, as Managing Director of Investor Growth Capital, and as a General Partner at Panorama Capital, L.P., a venture capital fund. Earlier in his career, Dr. Aggarwal was an associate with JPMorgan Partners, LLC, a private equity division of JPMorgan Chase & Co. Dr. Aggarwal previously served on the Boards of Directors of Hyperion Therapeutics, Inc. (acquired by Horizon Pharma plc) and Microlin Bio, Inc. and on several privately held biopharmaceutical companies. Dr. Aggarwal received his M.D. from Columbia University, College of Physicians & Surgeons, and his B.S. in Agricultural Economics from Cornell University.

Josh Richardson, M.D., has served as Managing Director of Longitude Capital since February 2016 where he focuses on investments in biotechnology companies. From September 2014 to February 2016, Dr. Richardson served as a Public Equities Analyst at HealthCor Management where he managed small and mid-cap biotechnology investments. Dr. Richardson received his B.S. in Biomedical Science from the University of South Florida, and his M.D. from the University of Virginia.

Mona Ashiya, Ph.D, is currently a Partner at OrbiMed Advisors, LLC, a healthcare focused investment firm. She has been at OrbiMed since 2010 where she has been involved with a number of investments in public and private biotech companies. Dr. Ashiya received her B.A. from the University of California, Berkeley and her Ph.D. in Cellular, Molecular and Developmental Biology from the University of Pittsburgh.

Andrew Sinclair, Ph.D., has served in various positions since November 2008 at Abingworth LLP, a life sciences investment group, where he currently serves as a Partner and Portfolio Manager. Dr. Sinclair currently serves on the Boards of Directors of Soleno Therapeutics, Inc. and Verona Pharma plc. Dr. Sinclair is a member of the Institute of Chartered Accountants in England and Wales. Dr. Sinclair received his B.Sc. in Microbiology from King’s College London and his Ph.D. in Chemistry and Genetic Engineering at the BBSRC Institute of Plant Science, Norwich.

The public offering of Series A convertible preferred stock, together with Series A warrants and Series B warrants, each to purchase shares of common stock, provided Sierra Oncology with net proceeds of approximately $98.0 million, after deducting underwriting discounts and commissions and offering expenses. Following the closing of the offering, and after giving effect to (i) the previously-announced issuance of shares of common stock and a warrant to purchase common stock to Gilead Sciences, Inc. (Gilead) in consideration for amending the royalty rates and milestones in an Asset Purchase Agreement with Gilead for momelotinib, subject to certain conditions, and (ii) the conversion of shares of Series A convertible preferred stock into shares of common stock that will occur following stockholder approval of a reverse stock split the company expects to conduct, but before giving effect to such reverse stock split, there are expected to be 415,786,654 total shares of common stock outstanding and warrants to purchase 444,088,071 total shares of common stock outstanding.