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Identifying branded drugs with a low likelihood of generic entry has become a crucial strategy for companies looking to expand their product portfolio through in-licensing. This approach not only helps maintain market exclusivity but also ensures a steady revenue stream for pharmaceuticalcompanies.
a leading global provider of immuno-oncology imaging agents, today announced it has signed a new multi-year, non-exclusive license with Pfizer Inc. ImaginAb will receive license fees and payments for manufacturing and other support. Working with leading pharmaceuticalcompanies such as Pfizer, will help us achieve our goal.”
These structures are particularly relevant in dealing with uncertainty about the future commercial potential of the target's products. This involves assessing the strength and breadth of patents, evaluating the potential for future patent challenges, and analyzing the value derived from licensing agreements and royalty streams.
Allecra, subject to the satisfaction of terms and conditions as set forth in the Exclusive Licensing Agreement, is to receive an upfront cash payment and is eligible to receive additional development and commercial milestone payments with an overall deal value of $78 million, in addition to royalties.
Purity and radioactive enrichment are key factors in ensuring the IS aligns with product specifications. For small- and medium-sized pharmaceuticalcompanies, outsourcing represents a strategic leap forward, offering a gateway to unparalleled expertise and cutting-edge analytical technologies.
15, 2020 (GLOBE NEWSWIRE) — Burning Rock Biotech Limited (NASDAQ: BNR, the “Company” or “Burning Rock”) today announced that it entered into an exclusive licensing agreement with Oncocyte Corporation (NYSE American: OCX) to bring DetermaRx , a risk stratification test for early stage lung cancer patients, to China.
1, 2020 /PRNewswire/ — Sosei Group Corporation (“the Company”) (TSE: 4565) announces it has entered into a global collaboration and license agreement with Biohaven Pharmaceutical Holding Company Ltd. (“Biohaven”, NYSE: BHVN). .
TOKYO and CAMBRIDGE, England , Dec. Vlad Coric , M.D.,
TOKYO & AUSTIN, Texas–( BUSINESS WIRE )– Taiho Pharmaceutical Co., Lung Tx”) announced today an exclusive license agreement of LTI-01 , a recombinant human single-chain urokinase plasminogen activator, currently under development by Lung Tx for loculated pleural effusions , for the territory of Japan.
Due to open source data’s accessibility, it is an appealing resource for drug research as it often enables cost-effective sources for emerging pharmaceuticalcompanies and academic research projects. Paid Knowledge Bases Paying for access or licensing a knowledge base can be a difficult decision to make.
03, 2021 (GLOBE NEWSWIRE) — EyePoint Pharmaceuticals, Inc. NASDAQ: EYPT), a pharmaceuticalcompany committed to developing and commercializing innovative ophthalmic products, today announced that Ocumension Therapeutics, a China-based ophthalmic pharmaceuticalcompany traded on the Stock Exchange of Hong Kong (1477.HK),
Under an exclusive licensing agreement with Endo International’s (NASDAQ: ENDP) subsidiary, Endo Ventures Limited, Par Pharmaceuticals’ Sterile Products division will launch and distribute the product. and Canada. and Canada. Founder, Chairman and Chief Executive Officer of Nevakar. .
Nevakar Inc.
Under the terms of the settlement agreements, AbbVie and Medytox will release all claims against Evolus related to the alleged misappropriation of Medytox’s trade secrets and grant a license to Evolus to continue to commercialize Jeuveau® in the United States and Nuceiva in all other territories in which Evolus has licensing rights.
21, 2020 (GLOBE NEWSWIRE) — TLC (Nasdaq: TLC, TWO: 4152), a clinical-stage, specialty pharmaceuticalcompany developing novel nanomedicines to target areas of unmet medical need, today announced the appointment of Thomas H. SOUTH SAN FRANCISCO, Calif. and TAIPEI, Taiwan, Oct.
“We look forward to accelerating the development of SPR206 in Asia and working closely with our partners at Spero Therapeutics to advance this novel product candidate for patients around the world with limited treatment options.” SHANGHAI , Jan. ” About SPR206. About Everest Medicines.
5, 2021 /PRNewswire/ — Sosei Group Corporation (“the Company”) (TSE: 4565) announces it is to regain the worldwide rights to its muscarinic agonist programs. The program was licensed to Allergan in April 2016 , and Allergan was acquired by AbbVie in May 2020. ” About the License Agreement.
28, 2021 /PRNewswire/ — CASI Pharmaceuticals (Formerly Known As EntreMed, Inc.). The Company’s validated, proprietary F.I.R.S.T biopharmaceutical company focused on developing and commercializing innovative therapeutics and pharmaceuticalproducts in China , the United States , and throughout the world.
At their option, the collaboration with the European affiliate of a global pharmaceuticalcompany has expanded to three active pharmaceutical ingredients (“API”s). We are well positioned for a productive 2021.”
The fully integrated pharmaceuticalcompany creates value through China’s specialty pharmaceutical markets with focus on iron deficiency, pain management and respiratory. Through its Shielded Living Therapeutics platform, the company is developing functional cures for chronic diseases. Noema Pharma .
Furthermore, data show that the class of drug substances being developed within AlzeCure’s platform, so-called gamma-secretory modulators, selectively affect the production of toxic Abeta-amyloid, without affecting the cleavage of other substrates that potentially play an important role in normal physiological function. in the brain.
05, 2020 (GLOBE NEWSWIRE) — Collegium Pharmaceutical, Inc. Nasdaq: COLL), a specialty pharmaceuticalcompany committed to being the leader in responsible pain management, today reported its financial results for the quarter ended September 30, 2020 and provided a corporate update. About Collegium Pharmaceutical, Inc.
Most have focused on patents specifically licensed to pharmaceuticalcompanies from academic institutions, where the vast majority of basic biological research takes place in America, most of it supported by NIH. The term NME refers to molecules that are unique among regulated or approved drug products in their mode of activity.
The process of transforming a therapeutic or technology from the research and development stage into a market-ready product or service is intricate and laden with obstacles. The university then licenses the IP to an existing pharmaceuticalcompany or a biotech startup, which takes on Investigational New Drug (IND) enabling studies.
George Yeh, President of TLC, commenced the conference and welcomed the company’s new Chief Business Officer, Mr. Tom Bliss. With experiences attained in licensing and business development functions from Amgen, Baxter and Johnson & Johnson, Mr. Bliss introduced himself in Mandarin Chinese. SOUTH SAN FRANCISCO, Calif.
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Vivera Pharmaceuticals, Inc., is an innovative, science-driven pharmaceuticalcompany focused on novel therapies for a variety of indications. Vivera is vertically integrated with patented technology, manufacturing capabilities, and distribution for its products.
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Sébastien Peltier, CEO of VALBIOTIS, and Jocelyn Pineau, CFO, are taking part in this key event for biotechnology and pharmaceuticalcompanies.
Its products are intended to be licensed to players in the health sector.
The Janssen PharmaceuticalCompanies of Johnson & Johnson announced two Phase III trials, DISCOVER-1 and 2 demonstrated Tremfya (guselkumab) improved fatigue in adults with active psoriatic arthritis (PsA). There was a handful of positive clinical trial news reported today. Here’s a look. Janssen’s Tremfya.
Tyvaso DPI, previously referred to as Treprostinil Technosphere ® , is an investigational drug-device combination product comprised of a dry powder formulation of treprostinil and a small, portable, dry powder inhaler. United Therapeutics is developing Tyvaso DPI under a collaboration and license agreement with MannKind Corporation.
NYSE American:PLX) (TASE:PLX), a biopharmaceutical company focused on the development, production and commercialization of recombinant therapeutic proteins produced by its proprietary ProCellEx ® plant cell-based protein expression system, and Chiesi Global Rare Diseases , a business unit of Chiesi Farmaceutici S.p.A.,
The sponsor is the pharmaceuticalcompany conducting the trial. Do you search for similar products, and use existing IND criteria requirements against the latest manufacturing guidance docs? A: Working in a pharmaceuticalcompany is the best way to learn this. A: This does not usually happen.
is a pharmaceuticalcompany conducting business in more than 70 countries around the world. Established in 2017, iota is a start-up company focused on building a foundation for the future of bioelectronic medicine. iota holds exclusive licenses to technologies developed at leading U.S. About Astellas. Astellas Pharma Inc.
MP0420 is subject to an option and license agreement with Novartis AG to develop, manufacture and commercialize Molecular Partners’ anti-COVID-19 DARPin® program. The DARPin® platform is a fast and cost-effective drug discovery engine, producing drug candidates with optimized properties for development and very high production yields.
Crist brings more than twenty years of oncology sales experience in both launch-stage and late-stage companies, building commercial organizations and developing high performing sales force teams. AVEO is an oncology focused biopharmaceutical company committed to delivering medicines that provide a better life for cancer patients.
More than thirty company-sponsored clinical studies covering more than fifteen indications have been conducted globally, including in China and the United States. Junshi Biosciences was the first Chinese pharmaceuticalcompany that obtained marketing approval for anti-PD-1 monoclonal antibody in China.
She has extensive experience in executive management, drug development, regulatory affairs and licensing with major international pharmaceuticalcompanies, including in the field of neurodegenerative diseases.
a publicly traded biopharmaceutical company, from 2012 to December 2019, managing its international, legal, quality, intellectual property and compliance functions, after serving in other executive roles at Acorda starting in 2004. Before joining Acorda, Ms. Shah also serves on the boards of several civic organizations and initiatives.
It increases the optionality to the Company’s value proposition, leverages our endocrine expertise and adds a late-stage pivotal trial-ready orphan disease product to the existing Phase 3 programs for abaloparatide and elacestrant,” said Radius Chief Executive Officer, Kelly Martin. Theresa Strong, Ph.D., ” Clinical Highlights.
“As our core business continues to perform well, we have a solid footing to enter 2021 with several key product launches including the potential INCREASE product label expansion for Tyvaso, the Remunity Pump for Remodulin, and the Implantable System for Remodulin,” said Martine Rothblatt , Ph.D., SILVER SPRING, Md.
To effectively navigate this ecosystem and expedite the development of new therapies, collaboration between the pharmaceutical industry and academia is proving increasingly vital. UC Berkeley claimed Genentech's product infringed on their broader patent, leading to a legal battle over ownership and royalties.
–( BUSINESS WIRE )– Aurinia Pharmaceuticals Inc. NASDAQ: AUPH / TSX:AUP) (“Aurinia” or the “Company”) today announced it has entered into a collaboration and license agreement with Otsuka Pharmaceutical Co., Learn more about Otsuka PharmaceuticalCompany on its global website at [link].
21, 2021 /PRNewswire/ — The Janssen PharmaceuticalCompanies of Johnson & Johnson today announced the U.S. Trademarks are owned by or licensed to Janssen and the ViiV Healthcare group of companies. CABENUVA offers adults living with HIV a new once-monthly injectable option for maintaining viral suppression.
By 2004, over a dozen companies were working on developing phage products and therapies, in locations ranging from Baltimore to Bangalore, where ten years previously, there had been none. Phage-based products have been licensed for use as antibacterial agents in the sanitation , food production , and animal health industries.
ASHP’s full suite of drug information has been integrated into and made available through DrugBank, bringing together both company’s offerings to provide streamlined access to a broader range of high quality products.
As our first NDA approved drug, Sesquient validates our business model of efficient development of critical care hospital injectable products,” added John Sedor, Chairman, CEO and co-founder of Sedor. Concurrently, Sedor is in discussions on securing capital to retain North American rights and commercialize the product.
Takeda PharmaceuticalCompany Limited ( TSE:4502/NYSE:TAK ) (“Takeda”) and Ovid Therapeutics Inc. I would like to thank Ovid for their thoughtful and productive collaboration. About Takeda PharmaceuticalCompany Limited. President of Research and Development at Takeda.
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