Moleculin Announces Outlicensing Deal To Accelerate Preclinical and Clinical Development

On February 20, 2019 Moleculin Biotech, Inc., (Nasdaq: MBRX) ("Moleculin" or the "Company"), a clinical stage pharmaceutical company focused on the development of oncology drug candidates, all of which are based on license agreements with The University of Texas System on behalf of the M.D. Anderson Cancer Center, reported that it has entered into a sublicense agreement with WPD Pharmaceuticals (WPD), located in Poland (Press release, Moleculin, FEB 20, 2019, View Source [SID1234533527]).

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The agreement provides WPD with exclusive rights, subject to current license agreements, to develop and market a range of Moleculin’s technologies in certain European countries (which does not include the UK, France, Italy and Spain) in exchange for contributing a minimum of $4 million in development expenditures agreed upon by Moleculin during the term of the agreement plus an ongoing royalty on future revenues. The agreement is specifically geared to provide Moleculin with the benefit of European Union (EU) grant funding, which is available to companies like WPD that are formed and present in EU countries.

The Company has previously entered into similar agreements with Dermin s.p. z.o.o. with some of its technologies in similar territories and Dermin has succeeded in obtaining grant funding in Poland benefiting the Company’s development objectives.

"Prior to being a public company, our portfolio benefited from funding obtained by Dermin in the past allowing us to accelerate our lead drug development in exchange for the rights to selected territories," commented Walter Klemp, Moleculin’s Chairman and CEO, "so, we already have a strong track record of pursuing and utilizing EU funding sources. Since our Scientific Founder, Dr. Waldemar Priebe has a major interest in both Moleculin and WPD, we believe we have an even better alignment of priorities allowing both companies to work together for our mutual benefit with this new agreement going forward."

Mr. Klemp added: "We view this as a potential source of ‘non-dilutive financing’ that we believe greatly benefits Moleculin shareholders. We estimate that the territories we are outlicensing represent approximately 10% of the worldwide spending on healthcare (as reported by the World Health Organization), and exclude key markets considered important to potential future outlicensing opportunities with ‘Big Pharma,’ so, we believe the opportunity to access $4 million and potentially significantly more in spending toward our development objectives, without dilution to shareholders, is a good deal for Moleculin. We believe this deal may allow us to pursue new indications for our lead drugs that otherwise would remain unexplored, which may ultimately increase our market opportunities and our chances for earlier drug approval. An added and extremely important benefit of this approach is that Moleculin doesn’t have to invest its own resources in establishing an EU-based infrastructure that would be required to access such grant funding of our own. We believe this deal continues our low overhead, capital efficient approach."

Roth Capital Partners rendered a fairness opinion to the Company’s board of directors in connection with the transaction with WPD.

Heron Therapeutics to Present at the 8th Annual Leerink Partners Global Healthcare Conference

On February 20, 2019 Heron Therapeutics, Inc. (NASDAQ: HRTX), a commercial-stage biotechnology company focused on improving the lives of patients by developing best-in-class treatments to address some of the most important unmet patient needs, reported that Barry Quart, Pharm.D., President and Chief Executive Officer of Heron Therapeutics, will participate in a fireside chat at the 8th Annual Leerink Partners Global Healthcare Conference on Wednesday, February 27, 2019, at 1:00 p.m. EST at the Lotte New York Palace Hotel (Press release, Heron Therapeutics, FEB 20, 2019, View Source [SID1234533544]).

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A live webcast of this presentation will be available on the Company’s website at www.herontx.com in the Investor Resources section. A replay of the presentation will be archived on the site for 60 days.

Veracyte Announces Participation in Upcoming Investor Conferences

On February 20, 2019 Veracyte, Inc. (Nasdaq: VCYT) reported that members of its management team will be participating in two upcoming investor conferences (Press release, Veracyte, FEB 20, 2019, View Source [SID1234533489]). Executives from the company will be meeting with investors at the BTIG MedTech, Life Science & Diagnostic Tools Conference 2019 on Wednesday, February 27, 2019, in Snowbird, Utah. There will not be a webcasted presentation.

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Bonnie H. Anderson, chairman and chief executive officer, is scheduled to present at the 8th Annual SVB Leerink Global Healthcare Conference in New York City on Friday, March 1, 2019 at 9:00 a.m. EST. A live audio webcast of the company’s presentation will be available by visiting Veracyte’s website at View Source A replay of the webcast will be available for 90 days following the conclusion of the live presentation broadcast.

Peloton Therapeutics Secures $150 Million in Series E Financing

On February 20, 2019 Peloton Therapeutics, Inc., a drug discovery and development company advancing first-in-class oral medicines for cancer and other serious conditions, reported the closing of an oversubscribed $150 million Series E financing (Press release, Peloton Therapeutics, FEB 20, 2019, View Source [SID1234533508]). The financing was led by RA Capital Management and was joined by new investors including Eventide Asset Management, Biotechnology Value Fund, OrbiMed, EcoR1 Capital, Vida Ventures, Curative Ventures and Driehaus Capital Management LLC. Peloton’s existing investors, including The Column Group, Nextech Invest Ltd, Topspin Fund LP, Tichenor Ventures LLC and Foresite Capital Management also participated in the financing.

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"We are delighted to have received such avid support from this eminent group of healthcare investors," said John Josey, Ph.D., Peloton’s Chief Executive Officer. "Proceeds from this financing will be used to advance Peloton’s research and development pipeline, including our lead drug candidate, PT2977, a potent and selective oral HIF-2α inhibitor."

"RA Capital is excited to support Peloton as it moves towards a Phase 3 trial of PT2977 for patients with metastatic renal cell carcinoma and pushes forward clinical development of this drug candidate in Von Hippel-Lindau disease, a familial cancer syndrome for which there are currently no approved drugs," said Derek DiRocco, Ph.D., Principal, RA Capital Management.

Sapreme Technologies in a 6.8 M€ EU Alliance to Develop an Oligonucleotide Delivery Platform Based on Its Proprietary Endosomal Escape Enhancers

On February 20, 2019 Sapreme Technologies, a privately-held biotech company developing a technology platform to enable the cytosolic delivery of macromolecule therapeutics, has been awarded a 6.8 M€ grant together with a multidisciplinary consortium including 11 other academic and industrial parties (Press release, Sapreme Technologies, FEB 20, 2019, View Source [SID1234538877]). The grant was provided by the European Union (EU) through Horizon 2020 to develop a non-viral based gene therapy using Sapreme’s proprietary endosomal escape enhancers.

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Ruben Postel, CSO of Sapreme Technologies, "We are pleased to see that the EU has recognized the great potential of the ENDOSCAPE project and the expert multi-disciplinary consortium developing a novel oligonucleotide delivery technology for treatment of cancer and haemophilia patients"

Ernst Geutjes, acting Managing Director, "The fact that the EU awarded the proposal with the maximum score demonstrates the potential of Sapreme’s proprietary endosomal escape enhancement technology as well as the exceptional quality of the proposal and the consortium spearheaded by Sapreme and Charité – Universitätsmedizin Berlin"