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BioWorld - Tuesday, April 14, 2026
Home » Eli Lilly and Co.

Articles Tagged with ''Eli Lilly and Co.''

Test tubes, dropper and capsules

Evotec inks $1B discovery deal with Lilly targeting metabolic disease

Jan. 18, 2022
By Nuala Moran
LONDON – Evotec SE put the biggest ever headline figure on one of its pharma drug discovery collaborations, announcing a $1 billion deal with Eli Lilly and Co. in metabolic diseases. The Hamburg, Germany-based company will be responsible for the discovery of drug candidates for the treatment of diabetes and chronic kidney disease against targets identified by Lilly or Evotec, or sourced externally. Lily has rights to up to five programs, to be developed in the partnership and to take on any subsequent development, clinical validation and commercialization activities. The collaboration initially runs for three years.
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Panel: Aduhelm win benefits AD space despite noise and hurdles

Jan. 11, 2022
By Randy Osborne
“There isn’t a better place to be” now than in Alzheimer’s disease (AD) drug development, said Phyllis Ferrell, global head of external engagement in AD and neurodegeneration at Eli Lilly and Co., during Biotech Showcase’s panel talk titled, “Aduhelm: Stimulating the Next Generation of AD Treatment.”
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John Lewis, CEO, Entos

Care of delivery: Entos strikes a $450M deal with Lilly

Jan. 6, 2022
By Lee Landenberger
The hinge of the new development deal between Entos Pharmaceuticals Inc. and Eli Lilly and Co. is also the core of Entos’ business: delivering a drug without significant toxicity. Development of the cargo is only part of the story in creating safe and effective medicine, Entos CEO John Lewis told BioWorld. “You have to have a safe and effective delivery system.”
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Access key ingredient in Paxlovid vs. molnupiravir

Dec. 27, 2021
By Mari Serebrov
The FDA went from zero to two oral antivirals to treat COVID-19 in the space of two days, granting emergency use authorizations last week to Pfizer Inc.’s Paxlovid and Merck & Co. Inc.-Ridgeback Biotherapeutics Inc.’s molnupiravir. Both five-day regimens are authorized for use, within five days of COVID-19 symptom onset, in individuals at high risk of progressing to severe disease, including hospitalization and death.
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Connecting puzzle pieces

Foghorn and Lilly’s Loxo agree to a $1.3B oncology deal

Dec. 13, 2021
By Lee Landenberger
Foghorn Therapeutics Inc. is receiving $300 million up front in cash in its new collaboration with Loxo Oncology at Lilly to develop oncology medicines. Foghorn could bring in up to $1.3 billion in development and commercialization milestones. In addition, Lilly will invest $80 million in Foghorn.
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Regor Therapeutics and Eli Lilly ink $1.55B collaboration and licensing deal

Dec. 13, 2021
By Doris Yu
Regor Therapeutics Group and Eli Lilly and Co. have inked a collaboration and licensing deal to co-develop therapies for metabolic disorders in a deal worth more than $1.5 billion. Under terms of the agreement, Lilly is gaining access to Regor IP to support its development of therapies for obesity and diabetes.
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Prices for state covered drugs in China to be slashed by an average of 61.7%

Dec. 6, 2021
By Doris Yu
Pharmaceutical companies in China will cut the prices for more than five dozen drugs by an average of 61.7% to get them on the latest version of the country’s National Drug Reimbursement List. The National Healthcare Security Administration released the new list on Dec. 3, 2021. The new list includes 74 new drugs, the vast majority of which are branded products without generic versions in China. Only seven of the new drugs on the list have generic versions.
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Bamlanivimab and etesevimab

Lilly pulls EU filing for COVID-19 antibody cocktail as authorities back rivals, US places $1.29B order

Nov. 3, 2021
By Richard Staines
Eli Lilly and Co. has withdrawn a filing for its COVID-19 antibody cocktail in Europe after health authorities backed rivals – the day after a $1.29 billion purchase of the same medicines from the U.S. government. Indianapolis-based Lilly began filing data from the combination of bamlanivimab and etesevimab in March to enable a fast authorization by the European Medicines Agency.
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Court: HRSA 340B letter ‘arbitrary and capricious’

Nov. 1, 2021
By Mari Serebrov
Biopharma scored a victory of sorts in the ongoing 340B war that’s pitting drug companies against the combined forces of hospital groups, contract pharmacies and the U.S. Department of Health and Human Services.
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Boehringer ordered to give 340B discounts to contract pharmacies

Oct. 6, 2021
By Mari Serebrov
Boehringer Ingelheim International GmbH is the latest drug company to come into the crosshairs of the U.S. Health Resources and Services Administration over its restrictions on giving 340B drug discounts to contract pharmacies.
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