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Eli Lilly Can't Slip Teva's Migraine Drug Patent Suit

IP Law 360

Drugmakers Eli Lilly and Co. and Teva Pharmaceuticals must take their patent dispute over rival migraine medications to a jury, a Massachusetts federal judge said Monday, denying the bulk of the companies' dueling motions for summary judgment.

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Meitheal Announces Exclusive Commercial Licensing Agreement for Insulin Biosimilars in the US

LexBlog IP

. (“Meitheal”) has entered into an exclusive licensing deal with Tonghua Dongbao Pharmaceutical Co., The agreement grants Meitheal and its parent company, Nanjing King-Friend Biochemical Pharmaceutical Co., THDB and NKF will jointly handle product development and supply.

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Recent Insulin Glargine Biosimilar Developments

LexBlog IP

On Monday the FDA approved Eli Lilly’s insulin glargine biosimilar Rezvoglar, a biosimilar to Sanofi’s Lantus. Lannett Company, Inc. Lannett is co-developing the product with partners within the HEC Group of companies. Rezvoglar is the second Lantus biosimilar insulin product approved in the U.S.,

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Where’s Waldo: Global Discovery and Finding a Corporation

Patently-O

Courts to obtain discovery in order to facilitate foreign litigation; with the pending global litigation between Eli Lilly and Novartis serving as our key example. One quirk is that the Novartis patents were not developed alongside the company’s Cosentyx product. In 2021, Lilly brought the case to the U.S.

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Biopharma Develops Antibody and Stem Cell Therapies in the Fight Against COVID-19

Bio Law Blog

While existing antivirals and anti-inflammatory drugs are undergoing clinical testing against COVID-19 now , biopharmaceutical companies are taking a variety of approaches to develop new therapies. These come from stem cell-focused companies, including Hope Biosciences , Celltex and Athersys.

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Federal Circuit Panel Holds Hatch-Waxman Venue Under the Second Prong of § 1400(b) is Based on Actions Related to ANDA Submission

Fish & Richardson Trademark & Copyright Thoughts

7] If a branded company initiates an infringement action against a generic company within 45 days of receiving notice of ANDA submission, this triggers a 30-month stay during which FDA cannot issue a final approval for the ANDA. [8] If a branded company gets venue wrong, it risks a motion to dismiss for improper venue.

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A Therapeutic Solution for COVID-19: Repurposing Existing Drugs

Bio Law Blog

Generally, viruses penetrate a host cell, co-opt the host-cell machinery to replicate their genome, assemble new viruses and then escape the cell to spread the infection. Drug repurposing is being aggressively pursued by the biopharmaceutical industry. Antiviral drugs aim to interrupt some part of the viral life cycle.

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