Deciphera Pharmaceuticals, Inc. to Present at the JMP Securities 2018 Life Sciences Conference

On June 13, 2018 Deciphera Pharmaceuticals, Inc. (NASDAQ:DCPH), a clinical-stage biopharmaceutical company focused on addressing key mechanisms of tumor drug resistance, reported that Michael Taylor, Ph.D., President and Chief Executive Officer, will present at the JMP Securities 2018 Life Sciences Conference on Wednesday, June 20, 2018 at 8:30 AM ET at the St. Regis in New York (Press release, Deciphera Pharmaceuticals, JUN 13, 2018, View Source [SID1234527291]).

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A live webcast of the event will be available on the "Events and Presentations" page in the "Investors" section of the Company’s website at View Source A replay of the webcast will be archived on the Company’s website for 90 days following the presentation.

BioLineRx to Participate at JMP Securities 2018 Life Sciences Conference

On June 13, 2018 BioLineRx Ltd. (NASDAQ: BLRX) (TASE: BLRX), a clinical-stage biopharmaceutical company focused on oncology and immunology, reported that its Chief Executive Officer, Philip Serlin, will participate in a panel discussion at JMP Securities 2018 Life Sciences Conference on Wednesday, June 20, 2018 at 3:30 p.m. (EDT) (Press release, BioLineRx, JUN 13, 2018, View Source;p=RssLanding&cat=news&id=2354358 [SID1234527290]). The conference will be held at St. Regis New York, NY.

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Details of the panel discussion are as follows:

Title: Combination Strategies in Immuno-Oncology

Description: Recent clinical and commercial success with immune checkpoint blockade and cell-based therapy approaches has resurrected intense scientific interest in cancer immunotherapy. With approaches ranging from immune cell mobilization to epigenetic modulation and metabolic conditioning, panel participants will discuss the opportunities afforded by the field as well as the challenges posed by it, and how their individual development strategies have been designed to maximize the chances of ultimate success in immuno-oncology.

Key topics slated for discussion include: Next-generation immuno-oncology therapeutics, novel targets (e.g., inhibitory checkpoints, co-stimulatory molecules, etc.), biomarker strategies, the future of combination therapies, and challenges associated with drug cost and coverage.

BioCryst Pharmaceuticals and Idera Pharmaceuticals to Present at the JMP Securities Life Sciences Conference

On June 13, 2018 BioCryst Pharmaceuticals, Inc. ("BioCryst") (NASDAQ:BCRX), and Idera Pharmaceuticals, Inc. ("Idera") (NASDAQ:IDRA), reported that they will be presenting at the JMP Securities Life Sciences Conference on Thursday, June 21, 2018 at 10:00 A.M. E.T (Press release, BioCryst Pharmaceuticalsa, JUN 13, 2018, View Source [SID1234527289]).

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Links to a live audio webcast and replay of this presentation may be accessed in the Investors section of BioCryst’s website at http://www.biocryst.com and in the Investors and Media section of Idera’s website at View Source

Nordic Nanovector Announces Betalutin® has been granted Fast Track designation in the US for Follicular Lymphoma

On June 12, 2018 Nordic Nanovector ASA (OSE: NANO) reported that the US Food & Drug Administration (FDA) has granted Fast Track designation to Betalutin (177Lu-lilotomab satetraxetan) for the treatment of patients with relapsed or refractory follicular lymphoma (FL) after at least 2 prior systemic therapies (Press release, Nordic Nanovector, JUN 12, 2018, View Source [SID1234553499]).

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Lisa Rojkjaer MD, Nordic Nanovector CMO, commented: "We are pleased to have been granted Fast Track designation for Betalutin. This designation is based on the promising safety and preliminary efficacy data in patients with relapsed/refractory indolent non-Hodgkin’s lymphoma from the first part of the LYMRIT 37-01 study, and highlights the potential of Betalutin to be a new therapeutic option for these patients. We are now focusing the PARADIGME trial on 3L CD20-refractory FL patients, a population in urgent need of new therapies, and look forward to working with the FDA to advance the development of Betalutin".

PARADIGME is a global randomised Phase 2b clinical trial comparing two Betalutin dosing regimens (15MBq/kg Betalutin following 40mg lilotomab pre-dosing; 20MBq/kg Betalutin following 100mg/m2 lilotomab pre-dosing) in 3L FL patients. PARADIGME aims to enrol 130 patients across 80-85 sites in approximately 20 countries.

The primary endpoint for the study is overall response rate (ORR) and secondary endpoints include duration of response (DoR), progression free survival (PFS), overall survival (OS), safety and quality of life. An initial efficacy and safety data read-out for PARADIGME is targeted for the first half of 2020.

About Fast Track designation

Fast Track is a process designed to facilitate the development and expedite the review of drugs to treat serious diseases and fill an unmet medical need. The purpose is to get important new drugs to the patient earlier. The designation provides the opportunity for more frequent meetings with the FDA over the course of drug development. In addition, the Fast Track programme allows for Rolling Review, which enables a company to submit individual sections of its Biologic License Application (BLA) for review as they are ready, rather than waiting until all sections of the BLA are complete, as well as for eligibility for Accelerated Approval and Priority Review if relevant criteria are met.

-End-

For further information, please contact:

IR enquiries Malene Brondberg, VP Investor Relations and Corporate Communications

Cell: +44 7561 431 762

Email: [email protected]

International Media Enquiries Mark Swallow/David Dible/Isabelle Andrews (Citigate Dewe Rogerson)

Tel: +44 207 638 9571

Email: [email protected]

About Betalutin

Betalutin is a tumour-seeking anti-CD37 antibody (lilotomab) conjugated to a low-intensity radionuclide (lutetium-177). CD37 is highly expressed in B-cell non-Hodgkin’s lymphoma (NHL), representing a novel therapeutic target. Betalutin is internalised in tumour cells and prolonged exposure of the nucleus to radiation destroys DNA leading to tumour cell death. Betalutin also has a crossfire effect limited to a radius of 40 cells, which destroys surrounding tumour cells. Betalutin has shown promising efficacy and tolerability in the Phase 1/2a LYMRIT 37-01 clinical study in relapsed/refractory follicular lymphoma (R/R FL) and is currently in a pivotal Phase 2b trial, PARADIGME, in third line (3L) FL patients who are refractory to standard-of-care anti-CD20-based therapy (including rituximab).

Helix BioPharma Corp. Announces Fiscal Third Quarter 2018 Results

On June 12, 2018 Helix BioPharma Corp. (TSX: HBP) (FRANKFURT: HBP) ("Helix" or the "Company"), a clinical stage
immuno-oncology company developing innovative drug candidates for the prevention and treatment of cancer, reported its financial results for its fiscal quarter ended April 30, 2018 (Press release, Helix BioPharma, JUN 12, 2018, View Source [SID1234527598]).

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FINANCIAL REVIEW
The Company recorded a net loss and total comprehensive loss of $2,147,000 ($0.02 loss per common share) and $2,913,000 ($0.03 loss per common share) for the three-month periods ended April 30, 2018 and 2017, respectively. For the nine-month periods ended April 30, 2018 and 2017, respectively, the Company recorded a net loss and total comprehensive loss of $7,105,000 ($0.07 loss per common share) and $8,819,000 ($0.10 loss per common share).

Research and development
Research and development costs for the three and nine-month periods ended April 30, 2018 totalled $1,435,000 and $5,095,000,respectively ($1,932,000 and $6,111,000 respectively for the three and nine-month periods ended April 30, 2017).

L-DOS47 research and development expenses for the three and nine-month periods ended April 30, 2018 totalled $1,029,000 and $4,039,000, respectively ($1,208,000 and $4,480,000 respectively for the three and nine-month periods ended April 30, 2017). L-DOS47 research and development expenditures relate primarily to the Company’s LDOS002 European Phase I/II clinical study in Poland, its LDOS001 Phase I clinical study in the U.S., preliminary expenditures related to the Company’s LDOS003 Phase II clinical study in Poland and the Ukraine and various other expenditures in support of the Company’s overall L-DOS47 program.

The Company’s LDOS001 clinical study has been facing patient enrolment challenges and as a result the Company most recently increased start-up activities to add 6 additional clinical study sites, with planned recruitment to begin mid-summer 2018. In addition, an accelerated dosing protocol has been approved to help accelerate the LDOS001 clinical study. On May 30th, 2018, the Company announced the completion of the third cohort and the initiation of enrollment in the fourth cohort of the LDOS001 clinical study. Enrolment in the Company’s LDOS002 clinical study was previously terminated due to lack of efficacy and the Company is currently awaiting the finalized reports. Given the limited cash resources, the Company has slowed down the previously committed LDOS003 clinical trial which the Company previously planned to commence enrolment in early 2018.

V-DOS47 research and development expenses for the three and nine-month periods ended April 30, 2018 totalled $133,000 and $310,000, respectively ($309,000 and $659,000 respectively for the three and nine-month periods ended April 30, 2017). For the three and nine-month periods ended April 30, 2018 the Company’s Polish subsidiary received grant funding of $144,000 and $344,000, respectively ($92,000 and $228,000 respectively for the three and nine-month periods ended April 30, 2017). The higher expenditures in the prior year mainly reflect the increase in staff and consulting agreements as the Polish subsidiary ramped up activities in the V-DOS47 program. The Company’s wholly owned subsidiary in Poland has entered into a grant funding agreement with the Polish National Centre for Research and Development for research and development expenditures associated with VDOS47.

CAR-T research and development expenses for the three and nine-month periods ended April 30, 2018 totalled $192,000 and $317,000 respectively ($259 and $259 respectively for the three and nine-month periods ended April 30, 2017). During the current fiscal year, the Company commenced development of novel CAR-T therapeutics and new antibody-based technologies for cellbased therapies. The Company’s CAR-T expenditures relate primarily to collaborative research activities with ProMab Biotechnologies Inc.

Corporate research and development expenses for the three and nine-month periods ended April 30, 2018 totalled $122,000 and $346,000 respectively ($170,000 and $672,000 respectively for the three and nine-month periods ended April 30, 2017). Corporate research and development expenditures mainly reflect wages and benefits and related expenses associated with corporate head office staff. The reduction mainly reflects lower wages because of cost cutting initiatives to reduce headcount and third-party consulting costs.

Trademark and patent related expenses for the three and nine-month periods ended April 30, 2018 totalled $70,000 and $308,000, respectively ($75,000 and $197,000 respectively for the three and nine-month periods ended April 30, 2017). The Company continues to ensure it adequately protects its intellectual property.
Operating, general and administration Operating, general and administration expenses for the three and nine-month periods ended April 30, 2018 totalled $686,000 and $1,856,000, respectively ($944,000 and $2,826,000 respectively for the three and nine-month periods ended April 30, 2017). The decrease in operating, general and administration expenses reflects the Company’s cost cutting initiatives. The Company
eliminated the employment arrangement with its then CEO, who was also a director of the Company, and let go of its controller as part of a headcount reduction plan. Aggressive steps were also taken to reduce unnecessary expenditures such as travel, conferences, etc.…. In addition, various third-party contracts were also eliminated. During the fiscal quarter, the Company hired Deloitte as strategic advisor to explore partnering and licensing opportunities. Cost reductions taken at the head office were partially offset by operating, general and administrative expenditures being incurred at the Company’s newly formed subsidiary in Poland which mainly reflect salaries and benefits, legal and accounting services and overhead costs associated with the administrative office.

The Company recorded a net loss and total comprehensive loss of $2,147,000 ($0.02 loss per common share) and $2,913,000 ($0.03 loss per common share) for the three-month periods ended April 30, 2018 and 2017, respectively. For the nine-month periods ended April 30, 2018 and 2017, respectively, the Company recorded a net loss and total comprehensive loss of $7,015,000 ($0.07 loss per common share) and $8,819,000 ($0.10 loss per common share).

As at April 30, 2018 the Company had a working capital deficiency of $1,915,000, a shareholders’ deficiency of $1,507,000 and a deficit of $162,395,000. As at July 31, 2017 the Company had a working capital deficiency of $504,000, shareholders’ deficiency of $17,000 and a deficit of $155,380,000.
The Company continues to work with vendors to manage its cash position while ensuring vendors continue providing services while being paid, albeit over a longer period of time than previously agreed terms. The Company has raised approximately $6,913,000 from private placement financings during the current fiscal year. Nevertheless, the Company’s cash reserves of $770,000 as at April 30, 2018 in addition to the subsequent private placement on June 7, 2018 for gross proceeds of approximately $941,000 are insufficient to meet anticipated cash needs for working capital and capital expenditures through the next twelve months, nor are they sufficient to see the current or any planned research and development initiatives through to completion.

Though the funds raised have somewhat assisted the Company in dealing with its working capital deficiency and attempts to make vendors current, additional funds are required to advance the various clinical and preclinical programs, pay for the Company’s overhead costs and its past due vendors. To the extent that the Company does not believe it has sufficient liquidity to meet its current obligations, management considers securing additional funds, primarily through the issuance of equity securities of the Company, to be critical for its development needs.
Additional information can be found about the Company’s liquidity and capital resources in the Company’s Management

Discussion and Analysis.
The Company’s condensed unaudited interim consolidated statement of net loss and comprehensive loss for the three and ninemonth periods ending April 30, 2018 and 2017 and the condensed unaudited interim consolidated statement of cash flows for the nine-month periods ending April 30, 2018 and 2017