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BioBuzz announces the launch of the BioHive

By News Archive

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In case you haven’t heard, BioBuzz just announced the launch of the BioHive – an Online Community and Collaboration Platform that is now open to general public. The BioHive will help enable all the components in our regional biotech ecosystem to work more efficiently to accelerate innovation, collaboration, workforce and growth opportunities.

Categorized into industry specific networks, the BioHive was built to bring together this region digitally and cultivate relationships that otherwise would not have been created due to company, role, geography, etc.

Please help us by pointing your coworkers and peers to the BioHive tab at http://www.biobuzz.net/ or directly at https://biohive.breezio.com to learn more and register for free today for their own BioHive account.

Working to build a stronger Biotech community has been BioBuzz’s mission for more than six years, so they are very excited to bring to you this great resource – so come join me on the BioHive!

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Symbiomix Therapeutics Accelerates Commercial Launch Preparation for Solosec™ Following Presentation of Results from Second Pivotal Trial at IDSOG

By News Archive

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Symbiomix today announced it is accelerating plans for the commercial launch of Solosec™ (secnidazole) oral granules following the presentation of clinical results from the second pivotal trial for the treatment of bacterial vaginosis (BV) with the hiring of Taunia Markvicka, PharmD, MBA, as Chief Commercial Officer. Symbiomix had a significant presence at the Infectious Diseases Society for Obstetrics and Gynecology (IDSOG) Annual Meeting in Annapolis, Maryland this past weekend with both the oral data presentation and sponsorship of a panel discussion on emerging diagnosis and treatment recommendations for BV. In addition, the company announced that the U.S. Food and Drug Administration (FDA) issued conditional acceptance of the proprietary name Solosec™. Solosec™ was previously known as SYM-1219.

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Maryland Life Sciences Advisory Board is Seeking Your Input

By News Archive

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The Maryland Life Sciences Advisory Board (LSAB) is developing recommendations to support the continued growth of the BioHealth industry in Maryland. The LSAB Working Group focused on Workforce and Access to Talent is seeking your input for their recommendations.

If you are involved with hiring/training employees, please take five minutes to complete this online survey by next Monday, August 22nd to have your feedback considered by the LSAB Workforce Working Group. (Please forward this survey to your HR manager/others if appropriate.)

Your input is valued. All responses will be kept confidential unless you ask for a member of the LSAB to contact you. If you have any questions or feedback for the other groups (Access to Capital, Technology Transfer, Foundational Support, Convergence of Bio and IT), please email the Maryland Department of Commerce at biohealth.info@maryland.gov.

Thank you for sharing your time and feedback.  

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Leidos Closes on Lockheed Martin’s IT Business – Nextgov.com

By News Archive

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Defense IT firm Leidos today announced it has successfully closed on the acquisition of Bethesda, Maryland-based Lockheed Martin’s Information Systems & Global Solutions business, formalizing a deal announced in January.

With Lockheed Martin’s $5 billion IT business, Leidos becomes the government’s largest IT provider—nearly doubling its annual revenue to $10 billion—and further cements its place as a force in the growing federal health IT market.

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Precision medicine’s chicken and egg problem – MedCity News

By News Archive

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Companion diagnostics is gaining currency as novel drugs are being paired up with tests that determine which patients will have a higher chance of  responding to that drug.

But 15 years after the human genome project has been completed, the progress of precision medicine appears to be woefully slow, at least according to Nicholas Dracopoli, vice president and head of Oncology Biomarkers at Janssen Research & Development, part of Johnson & Johnson. Others believe precision medicine and companion diagnostics have a chicken and egg problem.

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Tioma Therapeutics Announces $86 Million Series A Financing

By News Archive

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Tioma Therapeutics, Inc., a venture-stage biopharmaceutical company developing anti-CD47 antibodies for the treatment of solid and hematologic cancers, today announced it has raised $86 million in Series A venture financing. Proceeds from this financing will be used to further develop Tioma’s antibody portfolio, including its lead drug candidate — an anti-CD47 immune checkpoint inhibitor — through advanced proof-of-concept in human clinical trials.

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QIAGEN announces plans to return approximately $250 million to shareholders via synthetic share repurchase proposal

By News Archive

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QIAGEN N.V. (NASDAQ: QGEN; Frankfurt Prime Standard: QIA) today announced plans to return approximately $250 million to shareholders through a synthetic share repurchase proposal that combines a direct capital repayment with a reverse stock split.

These actions, which will lead to an adjustment in QIAGEN’s share capital, have been used previously by other large, multinational Dutch companies as an efficient way to provide returns to shareholders. The proposal, if adopted, is expected to be similar to QIAGEN repurchasing approximately $250 million of its own shares, but will enable the return of capital to all shareholders in a much faster and more efficient way than through a traditional open-market repurchase program.

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Peter Ronco

By Uncategorized

CEO Emmes & PE Board Advisor

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Peter is an accomplished drug developer and innovative senior pharmaceutical executive who is currently the CEO of Emmes as well as advising boards, private equity investors, and leaders across the pharmaceutical and biotech industry.  He has extensive global experience across a broad range of therapeutic areas, including oncology, immunology, neuroscience, vaccines, anti-infectives, cardiovascular and retinal gene therapy – from First in Human to Medical Affairs.

In his current role as CEO of Emmes, he is responsible for setting both the strategic direction and the day-to-day operations of the full service CRO operating in 30+ countries and across multiple disease areas including ophthalmology, vaccines, rare disease, cell & gene therapy, and neuroscience.  Emmes is collaborating with more than 210 sponsors, within the pharmaceutical/biotech industry, government, including over a dozen institutes of the National Institutes of Health (NIH), academic organizations, and non‐profit foundations.

Until January 2023, Peter was the Head of Global Development at Janssen R&D where he was responsible for leading the Global Development organization (including statistics, clinical pharmacology, clinical operations, data operations, project and portfolio management, etc.) in support of delivering a broad ranging portfolio of 450+ studies across all therapeutic areas and all phases from PhI -IV. In this role he managed a 10,000+ globally distributed organization and a $2bn+ operating budget to support the design of innovative drug development programs and the implementation of innovative approaches to trial design and execution including trial virtualization, digital health, patient-centered research, and diversity in clinical trials.

Prior to joining Janssen in 2017, Peter was the Senior Vice President of Global Clinical Operations at Bristol Myers-Squibb where he had spent 14 years holding positions of increasing leadership scope in Medical Affairs, Regulatory Operations and R&D Operations.  He also served on the TransCelerate Biopharmaceutical Board of Directors.  Prior to joining BMS, Peter was a consultant with Accenture, focusing on post-merger integration of R&D organizations.  He is a graduate of Nottingham University in the UK and lives in Chester, NJ.

 

 

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