Veracyte to Present at the William Blair 38th Annual Growth Stock Conference

On May 30, 2018 Veracyte, Inc. (Nasdaq: VCYT) reported that Bonnie H. Anderson, chairman and chief executive officer, will present at the William Blair 38th Annual Growth Stock Conference on Wednesday, June 13, 2018 at 12:40 p.m. Central Time in Chicago, IL (Press release, Veracyte, MAY 30, 2018, View Source [SID1234526955]).

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The live webcast of the presentation and a subsequent replay may be accessed by visiting Veracyte’s website at View Source The replay of the webcast will be available shortly after the conclusion of the presentation and archived on the company’s website for 90 days following the presentation.

AzurRx Announces Appointment of Dr. James Pennington as Chief Medical Officer

On May 30, 2018 AzurRx BioPharma, Inc. (NASDAQ:AZRX) ("AzurRx" or the "Company"), a company specializing in the development of non-systemic, recombinant therapies for gastrointestinal diseases, reported the appointment of Dr. James Pennington as the Company’s Chief Medical Officer (Press release, AzurRx BioPharma, MAY 30, 2018, View Source [SID1234526949]).

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"We are delighted to welcome Jim to the senior management team as we rapidly advance our clinical programs," commented Thijs Spoor, CEO of AzurRx BioPharma. "Jim is a highly accomplished pharmaceutical industry executive with extensive medical and clinical experience, as well as hands-on experience in regulatory affairs. His appointment is timely as 2018 is shaping up to be a pivotal year for AzurRx, with a number of upcoming and potentially value enhancing milestones including the initiation of the MS1819 Phase 2 study in cystic fibrosis patients and the filing of the investigational drug application ("IND") in the U.S. for MS1819. We look forward to Jim’s leadership and contributions as these programs move forward."

"I am excited to join the AzurRx team at this exciting time for the Company," said Dr. Pennington. "We look forward to initiating a cystic fibrosis study later this year. MS1819, which has generated promising interim results in the ongoing study in chronic pancreatitis patients, addresses a billion-dollar market in exocrine pancreatic insufficiency. It has the potential to become best in class due to the high pill burden, patient compliance issues, and manufacturing/supply chain challenges of the current animal-derived therapies."

Dr. Pennington brings over 30 years of experience in the pharmaceutical industry. He served as Vice President at Bayer Corporation where, under his direct supervision, Bayer received ten product approvals from the U.S. Food & Drug Administration ("FDA") and ten product approvals from foreign regulatory authorities. Dr. Pennington also held senior positions at multiple therapeutics companies, including CMO roles at Anthera Pharmaceuticals and CoTherix Inc. and Senior VP of Research, Development and Clinical Affairs at Alpha Therapeutics Corp. Dr. Pennington has participated in many FDA pre-IND meetings and has also participated in several FDA Advisory Panel meetings. He has served on various editorial boards as well as professional societies, such as the American Association of the Advancement of Science. He is involved in academia and is currently Clinical Professor of Medicine at the University of California in San Francisco. Dr. Pennington holds a B.A. from the University of Oregon and an M.D. from the University of Oregon Medical School and is Board Certified in internal medicine and infectious diseases.

Sangamo Therapeutics Announces Presentation At The 2018 Jefferies Global Healthcare Conference

On May 30, 2018 Sangamo Therapeutics, Inc. (Nasdaq: SGMO) reported that management will present a corporate overview at the 2018 Jefferies Global Healthcare Conference in New York City (Press release, Sangamo Therapeutics, MAY 30, 2018, View Source [SID1234526968]). The presentation is scheduled for Wednesday, June 6th at 4:30 p.m. ET.

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The presentation will be webcast live and may be accessed via a link on the Sangamo Therapeutics website in the Investors and Media section under Events and Presentations. The presentation will be archived on the Sangamo website following the event.

Selecta Biosciences to Present at the Jefferies Global Healthcare Conference on June 06, 2018

On May 30, 2018 Selecta Biosciences, Inc. (Nasdaq:SELB), a clinical-stage biopharmaceutical company focused on unlocking the full potential of biologic therapies by mitigating unwanted immune responses, reported that CFO and Head of Corporate Strategy John Leaman, M.D., will present at the Jefferies Global Healthcare Conference in New York City at 10:30 a.m. ET on Wednesday, June 06, 2018 (Press release, Selecta Biosciences, MAY 30, 2018, View Source [SID1234527006]). A live and archived webcast of the presentation can be accessed via the Investors & Media section of the company’s website, View Source

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Helix BioPharma Corp. Completes Third Dosing Cohort and Initiates Enrollment of the Next Cohort in U.S. Combination Treatment Study of Its Lung Cancer Drug Candidate L-DOS47

On May 30, 2018 Helix BioPharma Corp. (TSX, FSE: HBP) ("Helix" or the "Company"), an immuno-oncology company developing innovative drug candidates for the prevention and treatment of cancer, reported that the Safety Review Committee ("SRC") reviewed safety data from the third dosing cohort of the Company’s LDOS001 study and recommended that Helix begin enrollment of patients into the fourth dosing cohort (Press release, Helix BioPharma, MAY 30, 2018, http://www.helixbiopharma.com/helix-biopharma-corp-completes-third-dosing-cohort-initiates-enrollment-next-cohort-u-s-combination-treatment-study-lung-cancer-drug-candidate-l-dos47/ [SID1234527251]). LDOS001 is a dose escalation study of L-DOS47 with pemetrexed and carboplatin in recurrent or metastatic non-squamous non-small cell lung cancer. Patients enrolled in the fourth dosing cohort will receive the next L-DOS47 dose level which is 3.0 micrograms of L-DOS47 per kilogram of patient body weight.

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"We are very encouraged that L-DOS47 in combination with chemotherapeutics continues to be safe and well tolerated by patients," said Heman Chao, Helix’s Chief Executive Officer. "We look forward to completing this trial under an FDA approved amendment to accelerate dose escalation for this trial".

The following is an update regarding the LDOS001 trial:

 No dose limiting toxicities reported at doses up to 1.5 µg/kg (cohort 3)

 From imaging data available on the first nine patients, four confirmed partial response have been observed with one patient achieving a tumor volume reduction of 91%
 Eight additional patients to complete the study if no dose limiting toxicity is observed or cohort expansion is required due to safety concern