Array BioPharma To Present at the Jefferies 2018 Global Healthcare Conference

On May 30, 2018 Array BioPharma Inc. (Nasdaq:ARRY) reported that its Chief Executive Officer, Ron Squarer, will speak at the Jefferies 2018 Global Healthcare Conference in New York (Press release, Array BioPharma, MAY 30, 2018, View Source [SID1234527438]). The public is welcome to participate in the conference through a webcast on the Array BioPharma website.

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Event:

Jefferies 2018 Global Healthcare Conference

Presenter:

Ron Squarer, Chief Executive Officer, Array BioPharma

Date:

Wednesday, June 6, 2018

Time:

2 p.m. Eastern Time

Webcast:

View Source

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

Symphogen further strengthens its immuno-oncology pipeline by advancing into two additional clinical trials

On May 30, 2018 Symphogen, a private clinical late-stage antibody oncology focused biopharmaceutical company with a novel and differentiated antibody mixture pipeline, reported that it has enrolled the first patients into two separate Phase 1 clinical trials with two new investigational antibody therapies discovered from its immuno-oncology (I-O) activities with Shire targeting LAG3 (Sym022) and TIM3 (Sym023) (Press release, Symphogen, MAY 30, 2018, View Source [SID1234527007]).

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These are the second and third clinical programs to have been initiated under the I-O activities, the first being a Phase 1 trial of Sym021, an anti-PD1 antibody discovered by Symphogen, for solid tumors or lymphomas. All three I-O programs result from Symphogen’s antibody discovery and development activities under a strategic agreement with Shire plc established in 2016.

The Phase 1 clinical trials for each of these investigational therapies are open-label, dose-escalation studies designed to evaluate the preliminary safety and tolerability of the monotherapies in patients with locally advanced/unresectable or metastatic solid tumors or lymphomas that are refractory to available therapy or for which no standard therapy is available (Sym021: NCT03311412; Sym022: NCT03489369; Sym023: NCT03489343). Data is expected to be available in early 2019.

Commenting on the announcement, Chief Executive Officer of Symphogen, Martin Olin, said:
"We are excited about these important additions to our clinical pipeline. Our ability to advance three important immune checkpoint inhibitors into clinical development within a short period of time further validates the quality and the productivity of our antibody platform to rapidly generate unique antibody therapeutics that may enable new and improved treatment options for cancer patients. We now have seven product candidates in clinical development targeting important unmet medical needs demonstrating the potential significant value of our antibody platform. Our agreement with Shire provides the opportunity to bring next generation immunotherapies to patients for the treatment of cancer that could potentially be used in combination."

About the I-O programs
Symphogen’s research and development activities in the I-O area are focused on employing its antibody discovery and screening methodology against a number of targets demonstrated to be involved in cancer development and progression via negative regulation of the immune system, such as immune checkpoints found on immune cells. PD1, LAG3 and TIM3 are immune checkpoints playing important roles in regulating immune responses, including the body’s immune response to tumor cells (NEJM 2015; 2006-17, NEJM 2015; 372, 2509-20 and Nat Rev Drug Discovery 14; 561-584; 2015).

Sym021 is a novel, high affinity, chicken-derived, humanized antibody against PD1 with promising anti-cancer potential demonstrated in mouse tumor models. Sym022 is a novel antibody against LAG3, which shows enhanced anti-cancer activity in combination with anti-PD1 antibody therapy. Sym023 is an anti-TIM3 antibody with a novel mode of action.

Preclinical data for Sym021, Sym022 and Sym023 were presented at the recent American Association for Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting 2018 (Sym021: Abstract #3822; Sym022: Abstract #5626; Sym023: Abstract #5629).

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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Perrigo to Present at the Jefferies 2018 Healthcare Conference

On May 30, 2018 Perrigo Company plc (NYSE; TASE: PRGO) reported that Ron Winowiecki, Perrigo Chief Financial Officer, will present at the Jefferies 2018 Healthcare Conference at 8:30 AM EST on Tuesday, June 5, 2018 (Press release, Perrigo Company, MAY 30, 2018, View Source [SID1234527002]). Interested parties can access the presentation webcast at View Source

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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