Myovant Sciences to Present at the 38th Annual J.P. Morgan Healthcare Conference

On January 6, 2020 Myovant Sciences (NYSE: MYOV), a healthcare company focused on developing innovative treatments for women’s health and prostate cancer, reported that Lynn Seely, M.D., Myovant’s CEO, will present at the 38th Annual J.P. Morgan Healthcare Conference on Wednesday, January 15, 2020 at 7:30 a.m. Pacific Time in San Francisco, California (Press release, Myovant Sciences, JAN 6, 2020, https://investors.myovant.com/news-releases/news-release-details/myovant-sciences-present-38th-annual-jp-morgan-healthcare [SID1234552737]).

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A live webcast of the presentation will be accessible on the Events page under the Investors & Media section of the Myovant website at www.myovant.com. Please connect to the company’s website at least 15 minutes prior to the presentation to ensure adequate time for any software download that may be required to listen to the webcast. A replay of the webcast will be available at the same location for 30 days following the conference.

Moderna to Provide Business and Pipeline Updates at the 2020 J.P. Morgan Healthcare Conference

On January 6, 2019 Moderna, Inc., (Nasdaq: MRNA) a clinical stage biotechnology company pioneering messenger RNA (mRNA) therapeutics and vaccines to create a new generation of transformative medicines for patients, reported that CEO Stéphane Bancel will present an update on the Company and its pipeline of mRNA development programs at this year’s 38th annual J.P. Morgan Healthcare Conference (Press release, Moderna Therapeutics, JAN 6, 2020, View Source [SID1234552736]).

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Mr. Bancel’s presentation will take place on Monday, January 13, 2020 at 4:30 p.m. PT in the Colonial Room at The Westin St. Francis Hotel in San Francisco. The presentation will be followed by a question and answer session. A live webcast of both the presentation and question and answer session will be available under "Events & Presentations" in the investors section of Moderna’s website at View Source A replay of the webcast will be archived on Moderna’s website for 30 days following the presentation.

Akebia Therapeutics to Present at the 38th Annual J.P. Morgan Healthcare Conference

On January 6, 2020 Akebia Therapeutics, Inc. (Nasdaq: AKBA), a biopharmaceutical company focused on the development and commercialization of therapeutics for people living with kidney disease, reported that its President and Chief Executive Officer, John P. Butler, will present at the 38th Annual J.P. Morgan Healthcare Conference on Wednesday, January 15, 2020 at 9:30 a.m. PT in San Francisco (Press release, Akebia, JAN 6, 2020, View Source [SID1234552735]).

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A live webcast and replay of Akebia’s presentation and associated Q&A will be available on the Company’s website at www.akebia.com.

CStone Pharmaceuticals and Blueprint Medicines Initiate Phase 1b/2 Clinical Trial of Fisogatinib in Combination with CS1001 for Patients with Hepatocellular Carcinoma

On January 6, 2020 CStone Pharmaceuticals ("CStone", HKEX: 2616), a biopharmaceutical company focused on developing and commercializing immuno-oncology and precision medicines, and Blueprint Medicines Corporation (NASDAQ: BPMC), a precision therapy company focused on genomically defined cancers, rare diseases and cancer immunotherapy, reported the dosing of the first patient in a Phase 1b/2 trial evaluating fisogatinib in combination with CS1001 for the treatment of locally advanced or metastatic hepatocellular carcinoma (HCC) (Press release, CStone Pharmaceauticals, JAN 6, 2020, View Source [SID1234552734]). The study will be conducted across multiple clinical sites in China, where according to GLOBOCAN data, nearly half of the world’s new HCC cases occurred in 2018.

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This trial will assess the potential for two complementary treatment approaches – precision therapy and immuno-oncology therapy – to enhance anti-tumor activity in locally advanced or metastatic HCC. Discovered by Blueprint Medicines, fisogatinib is an investigational, potent and highly selective inhibitor of fibroblast growth factor receptor 4 (FGFR4) in clinical development for the treatment of advanced FGFR4-driven HCC. CS1001 is an investigational anti-PD-L1 monoclonal antibody being developed by CStone for multiple tumor types. Preclinical studies in an HCC model have shown that treatment with fisogatinib stimulated T-cell infiltration into the tumor microenvironment, suggesting that combining fisogatinib with a PD-L1 inhibitor may enhance anti-tumor activity in patients with FGFR4-driven HCC.

Blueprint Medicines and CStone Pharmaceuticals have an exclusive collaboration and license agreement for the development and commercialization of fisogatinib and certain other drug candidates in Mainland China, Hong Kong, Macau and Taiwan. Blueprint Medicines retains development and commercial rights for these drug candidates in the rest of the world.

"The CStone collaboration has rapidly expanded our global development activities into the Asia-Pacific region, where our partner has deep experience working with leading academic centers and local regulatory authorities," said Andy Boral, M.D., Ph.D., Chief Medical Officer at Blueprint Medicines. "We look forward to advancing our fisogatinib clinical program by conducting a Phase 1b/2 trial in China, where the incidence of HCC is disproportionately high. Because fisogatinib has exquisite selectivity against an oncogenic driver, we believe this investigational treatment is well-positioned for combination therapy. Fisogatinib and CStone’s PD-L1 inhibitor CS1001 have complementary mechanisms of action that may offer durable clinical activity in patients with HCC."

"HCC is a particularly aggressive disease and China is currently faced with enormous challenges due to limited effective treatment options and poor prognosis in HCC patients at advanced stages," said Archie Tse, M.D., Ph.D., Chief Translational Medicine Officer at CStone. "CStone is committed to addressing unmet clinical needs through identifying potentially transformative combination regimens against complex cancers like HCC. We are pleased that through our dedicated efforts, we have successfully achieved the dosing of the first patient in the Phase 1b/2 trial of fisogatinib in combination with CS1001, which hopefully will bring meaningful clinical benefits to advanced HCC patients. CS1001 is one of CStone’s backbone immuno-oncology assets and multiple combination therapy trials with CS1001 have been carried out."

Data from Blueprint Medicines’ ongoing Phase 1 trial, which was published online in Cancer Discovery on October 1, 2019, showed that fisogatinib monotherapy was clinically active and well-tolerated in patients with heavily pretreated advanced HCC. These results support fisogatinib’s potential as the first molecular biomarker-driven targeted therapy in HCC.

A Phase 1 dose-escalation study of CS1001 has been completed in China. Phase 1 data published at the 22nd Annual Meeting of the Chinese Society of Clinical Oncology (CSCO 2019) has demonstrated sustained clinical benefits from CS1001 in multiple tumor types, including gastric cancer, esophageal cancer and microsatellite instability high/deficient mismatch repair (MSI-H/dMMR) solid tumors. Pooled safety data from the Phase 1b trial released at the European Society of Medical Oncology (ESMO) (Free ESMO Whitepaper) 2019 Congress (ESMO 2019) showed that CS1001 had a promising safety and tolerability profile. These data indicate CS1001’s therapeutic potential in multiple tumor types including HCC.

About HCC

Liver cancer is the second leading cause of cancer-related deaths worldwide, with HCC accounting for most liver cancers. The highest incidence of HCC occurs in regions with endemic hepatitis B virus, including Southeast Asia and sub-Saharan Africa. Nearly half of the world’s new HCC cases are diagnosed in China. Treatment options for patients with advanced HCC are limited, with currently approved therapies providing time to progression of three to seven months and an overall survival of nine to 13 months. FGF19 is the ligand that activates FGFR4, a receptor that promotes hepatocyte proliferation and regulates bile acid homeostasis in the liver. Blueprint Medicines estimates that approximately 30 percent of patients with HCC have tumors with aberrantly activated FGFR4 signaling.

About the Phase 1b/2 Clinical Trial of Fisogatinib in Combination with CS1001

The Phase 1b/2 clinical trial is an open-label study of fisogatinib in combination with CS1001 for the treatment of patients with locally advanced or metastatic HCC. The trial consists of two parts: a dose-escalation phase and a dose-expansion phase. The dose-escalation phase was designed to evaluate two doses of fisogatinib in combination with a fixed dose of CS1001. The objective of the dose-escalation phase is to identify the recommended Phase 2 dose that will be used in the dose-expansion phase.

Objectives of the trial include evaluating the safety, tolerability, pharmacokinetics and anti-tumor activity of the combination regimen. FGF19 expression will be determined at a central laboratory. The trial is designed to enroll approximately 50 patients across multiple sites in China. For additional information on the trial, please go to clinicaltrials.gov.

About Fisogatinib

Fisogatinib is an orally available, potent, irreversible inhibitor of FGFR4. Fisogatinib was specifically designed by Blueprint Medicines to inhibit FGFR4 with exquisite selectivity, thereby sparing the paralogs FGFR1, FGFR2 and FGFR3. Preclinical data has validated FGFR4 as an oncogenic driver for a subset of patients with advanced HCC.

Blueprint Medicines is developing fisogatinib, an investigational medicine, for the treatment of patients with FGFR4-activated HCC. The U.S. Food and Drug Administration has granted orphan drug designation to fisogatinib for the treatment of HCC.

About CS1001

CS1001 is an investigational monoclonal antibody directed against PD-L1 being developed by CStone. Authorized by the U.S. based Ligand Corporation, CS1001 is developed by the OMT transgenic animal platform, which can generate fully human antibodies in one step. As a fully human, full-length anti-PD-L1 monoclonal antibody, CS1001 mirrors natural G-type immune globulin 4 (IgG4) human antibody, which can reduce the risk of immunogenicity and potential toxicities in patients, potentially representing a unique advantage over similar drugs.

CS1001 has completed a Phase 1 dose-escalation study in China, in which the drug showed good tolerability. During Phase 1a and 1b stages of the study, CS1001 produced sustained clinical benefits in multiple tumor types.

CS1001 is being investigated in a number of ongoing clinical trials, including one Phase 1 bridging study in the U.S. In China, its clinical program includes one multi-arm Phase 1b study, two pivotal Phase 2 studies, and four Phase 3 studies for several tumor types. (Press release, CStone Pharmaceauticals, JAN 6, 2020, View Source [SID1234552734])

Seattle Genetics to Present at the J.P. Morgan Healthcare Conference

On January 6, 2020 Seattle Genetics, Inc. (Nasdaq:SGEN) reported that management will present at the 38th Annual J.P. Morgan Healthcare Conference on Monday, January 13, 2020 at 2:30 p.m. Pacific Time (Press release, Seattle Genetics, JAN 6, 2020, View Source [SID1234552733]). Both the presentation and question and answer session that follows at 3:00 p.m. will be webcast live and available for replay from Seattle Genetics’ website at www.seattlegenetics.com in the Investors section.

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