Gilead Sciences to Release Second Quarter 2019 Financial Results on Tuesday, July 30, 2019

On July 16, 2019 Gilead Sciences, Inc. (Nasdaq: GILD) reported that its second quarter 2019 financial results will be released on Tuesday, July 30, after the market closes. At 4:30 p.m. Eastern Time, Gilead’s management will host a conference call to discuss the company’s financial results for the second quarter 2019 and provide a business update (Press release, Gilead Sciences, JUL 16, 2019, View Source [SID1234537572]).

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The live webcast of the call can be accessed at the company’s Investors page at View Source Please connect to the company’s website at least 15 minutes prior to the start of the call to ensure adequate time for any software download that may be required to listen to the webcast. Alternatively, please call 877-359-9508 (U.S.) or 224-357-2393 (international) and dial the conference ID 8696029 to access the call. Telephone replay will be available approximately two hours after the call through 8:00 p.m. Eastern Time, August 1, 2019. To access the replay, please call 855-859-2056 (U.S.) or 404-537-3406 (international) and dial the conference ID 8696029. The webcast will be archived on www.gilead.com for one year.

Melinta Therapeutics Announces Preliminary Second Quarter 2019 Financial Results and Provides Corporate Update

On July 16, 2019 Melinta Therapeutics, Inc. (NASDAQ: MLNT), a commercial-stage company focused on the development and commercialization of novel antibiotics to treat serious bacterial infections, reported preliminary and unaudited financial results and provided a corporate update for the second quarter ended June 30, 2019 (Press release, Cempra, JUL 16, 2019, View Source [SID1234537564]).

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"Melinta’s preliminary second quarter 2019 results demonstrate that the actions taken to improve upon the Company’s operational and financial efficiencies are continuing to drive progress," said John H. Johnson, chief executive officer of Melinta. "As we enter into the third quarter of 2019, we remain focused on driving sales efforts, preparing for the potential Baxdela (delafloxacin) community-acquired bacterial pneumonia (CABP) approval and launch, while also continuing to identify additional ways to reduce expenses. We believe in the strength of our long-term strategy to best position Melinta for future success and remain committed to delivering upon our mission of leading the global fight against antimicrobial resistance and providing antibiotic solutions to patients and healthcare providers."

Preliminary Second Quarter 2019 Financial Results
Melinta anticipates that it will report net product sales of approximately $13.8 million for the second quarter of 2019, which is an increase of 51 percent over the second quarter of 2018 and an increase of 17 percent over the first quarter of 2019.

Melinta also expects to report quarter-end cash and cash equivalents of approximately $90 million, and the Company is targeting to reduce full-year 2019 operating expenses by approximately $70 million.

The figures in the foregoing sentences are all based upon preliminary estimates and remain subject to change as the Company finalizes its results for the second quarter of 2019.
The Company will announce its full second quarter 2019 financial results on August 7, 2019 at 8:30 a.m. ET and plans to host a conference call at that time.

Recent Corporate Updates

On July 10, The World Health Organization (WHO) added Vabomere (meropenem and vaborbactam) to its Essential Medicines List for its ability to target multidrug-resistant infections caused by pathogens deemed a "critical priority" by the WHO, including carbapenem-resistant Enterobacteriaceae

The U.S. Food and Drug Administration (FDA) recently accepted for priority review a supplemental New Drug Application (sNDA) for Baxdela (delafloxacin) seeking to expand the current indication to include adult patients with community-acquired bacterial pneumonia (CABP); the FDA has assigned a Prescription Drug User Fee Act (PDUFA) action date (proposed review deadline) of October 24, 2019

Sixteen scientific presentations and posters of portfolio and pipeline data have been accepted for presentation at the Infectious Diseases Society of America IDWeek 2019 meeting, being held October 1 – 6, 2019 in Washington, D.C. and at the American College of Chest Physicians (ACCP) CHEST Meeting, being held October 19 – 23, 2019 in New Orleans, LA

Second Quarter 2019 Conference Call and Webcast
Melinta’s earnings conference call for the second quarter of 2019 will be broadcast at 8:30 a.m. ET on August 7, 2019. Investors wishing to participate in the call should dial: 877-377-7553 and international investors should dial: 253-237-1151, using the conference ID# 5166674. A live webcast of the call will be available online from the Investor Relations section of the company website at www.melinta.com and will be archived there for 30 days. A telephone replay of the call will be available by dialing 855-859-2056 for domestic callers or 404-537-3406 for international callers and entering the conference ID# 5166674.

Heska Corporation Second Quarter 2019 Financial Results and Earnings Call Scheduled for August 6, 2019

On July 16, 2019 Heska Corporation (NASDAQ: HSKA – News; "Heska" or the "Company"), a provider of advanced veterinary diagnostic and specialty products, reported its second quarter 2019 financial performance in a press release on Tuesday, August 6, 2019 before the market opens and to host an earnings call to discuss the results at 9 a.m. MT / 11 a.m. ET on the same day (Press release, Heska, JUL 16, 2019, View Source [SID1234537562]).

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To access the conference call:

From within the United States, please dial 1-800-289-0438
From outside of the United States, please dial 1-323-794-2423
Reference Conference ID: 7297179

The earnings call will be webcast live from the Company’s website at View Source

A telephonic replay will be available beginning at 2 p.m. ET August 6 and will continue through 11:59 p.m. ET on Tuesday, August 20, 2019. The webcast will be archived on www.heska.com for 90 days.

To access the replay:

From within the United States, please dial 1-844-512-2921
From outside the United States, please dial 1-412-317-6671
Reference Replay Pin Number: 7297179

BioMarin to Host Second Quarter 2019 Financial Results Conference Call and Webcast on Thursday, August 1 at 4:30pm ET

On July 16, 2019 BioMarin Pharmaceutical Inc. (NASDAQ: BMRN) reported that Jean-Jacques Bienaimé, Chairman and Chief Executive Officer of BioMarin, will host a conference call and webcast on Thursday, August 1, at 4:30 p.m. ET to discuss second quarter 2019 financial results and provide a general business update (Press release, BioMarin, JUL 16, 2019, View Source [SID1234537561]).

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Dial-in Number
U.S. / Canada Dial-in Number: (866) 502-9859
International Dial-in Number: (574) 990-1362
Conference ID: 6989536

Replay Dial-in Number: (855) 859-2056
Replay International Dial-in Number: (404) 537-3406
Conference ID: 6989536

Interested parties may access a live audio webcast of the conference call via the investor section of the BioMarin website, www.biomarin.com. A replay of the call will be archived on the site for one week following the call.

GEMoaB appoints oncology expert Michael Pehl as Chief Executive Officer

On July 16, 2019 GEMoaB GmbH, a biopharmaceutical company focused on the discovery, development, manufacture and commercialization of next-generation immunotherapies for difficult-to-treat cancers, reported the appointment of Michael Pehl to the CEO with effect from 1 July 2019 (Press release, GEMoaB Monoclonals, JUL 16, 2019, View Source [SID1234537560]). This move reflects GEMoaB’s strategy of positioning itself as a fully integrated biotech company over the long term. GEMoaB relies on its strong scientific expertise as well as its solid foundation in research and development.

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"We are pleased that with Michael Pehl, an experienced leader in the field of oncology GEMoaB will be heading into the next phase of growth. Under his leadership, GEMoaB will further develop its proprietary immunotherapy platforms in clinical trials. These include the Affinity-Tailored Adapters for T-Cells (ATAC), such as GEM333 and GEM3PSCA, and cellular immunotherapy (UniCAR / RevCAR). This can significantly improve the prognosis of patients with intractable hematological and solid tumors, "said Professor Dr. Gerhard Ehninger , founder and co-owner of the company." I know Michael Pehlfor many years. He has a strong scientific background, immense experience and is well positioned to lead and develop GEMoaB with its exceptional people, broad pipeline and partnerships. "

Michael Pehl has more than 25 years of leadership experience in the international biotech industry and in oncology in the US and Europe. Prior to joining GEMoaB, as Chief Executive Officer of Immunomedics Inc., he led the implementation of the clinical development plan and regulatory filing for the core product sacituzumab-govetecan for the treatment of metastatic triple-negative breast cancer.

Previously, Michael Pehl was President of Oncology at Celgene, responsible for the Company’s global commercial and clinical development, medical strategy and operational implementation. During this time, he was instrumental in expanding the pipeline and steadily growing global business volume. His responsibility included the clinical development program, and the introduction of drugs such as lenalidomide (Revlimid ), pomalidomide (Pomalyst ; Imnovid ) and Enasidenib (IDHIFA ) for the treatment of hematological malignancies, nab-paclitaxel (Abraxane ) in solid tumors as well as luspatercept in myelodysplastic syndrome (MDS) and beta-thalassemia.

Prior to that, Michael Pehl held senior positions at Celgene as Senior Vice President, Global Marketing and Strategy; Head of Global Marketing; Head of Hematology Europe; Vice President Central and Eastern Europe & Middle East and General Manager Germany .

His biotechnology career began at AMGEN, where he held leadership positions at the German and European levels in oncology and nephrology.

"I am grateful that I have been given the opportunity to lead GEMoaB and work with its excellent team at an exciting time for the company," said Michael Pehl, "with its highly differentiated next-generation immunotherapy platforms and its promising preclinical and GEMoaB’s goal is to make GEMoaB, together with our partners and potential investors, a fully integrated biopharmaceutical company that will help improve the cancer outcomes of cancer patients in indications for which there are currently There are far too few treatment options. "

About the Affinity-Tailored Adapter for T-Cells (ATAC) Platform

The GEMoaB-owned platform of the ‘Affinity-Tailored Adapter for T-Cells’ is due to a high binding affinity for tumor antigens and a lower affinity for the CD3 antigen on the
T-effector cells are characterized, which in preclinical models, the auto-activation of T cells is avoided. In addition, the safety and tolerability of the therapy may be improved by the relatively short serum half-life of only 60 minutes. Using fully humanized antibodies reduces the potential immunogenicity risk even with continuous treatment. The first two compounds from the ATAC platform in clinical trials are GEM333 and GEM3PSCA. GEM333 is an ATAC with specific binding to CD3 and CD33 and is currently in clinical development for the treatment of CD33-positive relapsed / refractory acute myeloid leukemia (AML). (For more information, see View Source). GEM3PSCA is an ATAC with specific binding to CD3 and the PSCA antigen.

About UniCAR / RevCAR

To avoid possible therapy-related toxicities as well as limitations in the efficacy and production of current CAR-T therapies, GEMoaB GmbH has developed universal and modular CAR technologies called UniCAR and RevCAR. These genetically modified T cells can be repeatedly turned on and off by administering a so-called targeting module ("TM") .TMs are bispecific molecules against various antigens that bind UniCAR / RevCAR T cells to the malignant target cells After elimination of the corresponding TM, the UniCAR / RevCAR T cells switch off automatically.