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BioWorld - Thursday, April 16, 2026
Home » Eli Lilly and Co.

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

RNA strand

Lilly moves deeper into RNAi with $1.2B Sanegene obesity deal

Nov. 10, 2025
By Tamra Sami
No Comments
In a deal worth $1.2 billion, Suzhou Sanegene Bio Inc. and Eli Lilly and Co. are partnering to advance RNAi candidates for metabolic diseases based on Sanegene's tissue selective delivery technology.
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Lilly's amylin drug heads to phase III on strong weight loss data

Nov. 6, 2025
By Karen Carey
No Comments
Eli Lilly and Co.’s amylin receptor agonist, eloralintide, showed impressive weight loss and improved tolerability in phase II results reported at ObesityWeek 2025, setting the stage for a phase III trial to start next month. The once-weekly drug demonstrated superior mean weight reductions from 9.5% to 20.1% vs. only 0.4% for placebo over 48 weeks, with all treatment arms meeting the primary endpoint, mean percent change in body weight from the average baseline of 240.5 lbs. (109.1 kg).
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Wegovy and Zepbound autoinjectors

Lilly, Novo MFN deals expected to ‘democratize’ obesity drugs

Nov. 6, 2025
By Mari Serebrov
No Comments
Hailing it as a win-win and a historic step forward in fighting chronic disease, the Trump administration announced pricing agreements Nov. 6 with Eli Lilly and Co. and Novo Nordisk A/S that will expand the availability of the companies’ weight loss drugs by cutting prices and, for the first time, providing coverage for the drugs in obesity through Medicare and Medicaid.
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Insulin pen

Adocia’s Biochaperone Lispro phase III T1D data positive in China

Oct. 28, 2025
By Marian (YoonJee) Chu
No Comments
Adocia SA is looking to further apply its Biochaperone formulation technology to metabolic disorders, Olivier Soula, Adocia co-founder and CEO told BioWorld, the firm having recently gained positive top-line phase III results of Tonghua Dongbao Pharmaceutical Co. Ltd.’s THDB-0206 injection (Biochaperone Lispro) in diabetes patients in China.
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Insulin pen

Adocia’s Biochaperone Lispro phase III T1D data positive in China

Oct. 24, 2025
By Marian (YoonJee) Chu
No Comments
Adocia SA is looking to further apply its Biochaperone formulation technology to metabolic disorders, Olivier Soula, Adocia co-founder and CEO told BioWorld, the firm having recently gained positive top-line phase III results of Tonghua Dongbao Pharmaceutical Co. Ltd.’s THDB-0206 injection (Biochaperone Lispro) in diabetes patients in China.
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Syringe and capsules atop lab chart
Biopharma clinical updates August 2025

Phase III successes in August include Sjögren’s, myasthenia gravis

Sep. 30, 2025
By Amanda Lanier
No Comments
In August 2025, BioWorld logged 95 clinical trial updates across phases I to III, compared to 140 tracked in July and 254 in June. Among them, 15 phase III studies delivered positive results, while one trial each reported a failure and mixed outcome.
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Feet and scale

Pfizer M&A prospect Metsera heads to phase III with lead GLP-1

Sep. 30, 2025
By Karen Carey
No Comments
Phase IIb data of Metsera Inc.’s lead GLP-1 receptor agonist, MET-097i, showed significant weight loss and good tolerability, supporting a phase III start later this year, and validating Pfizer Inc.’s decision a week ago to buy the obesity-focused company for $7.3 billion.
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Syringe and capsules atop lab chart
Biopharma clinical updates August 2025

Phase III successes in August include Sjögren’s, myasthenia gravis

Sep. 29, 2025
By Amanda Lanier
No Comments
In August 2025, BioWorld logged 95 clinical trial updates across phases I to III, compared to 140 tracked in July and 254 in June. Among them, 15 phase III studies delivered positive results, while one trial each reported a failure and mixed outcome.
Read More
Approved label with medical icons, professional

Lilly’s SERD in late-stage breast cancer receives FDA approval

Sep. 26, 2025
By Lee Landenberger
No Comments
Eli Lilly and Co.’s oral selective estrogen receptor degrader (SERD) imlunestrant has been approved by the U.S. FDA for treating late-stage breast cancer patients. Branded Inluriyo, the second-line treatment is for treating adults with estrogen receptor-positive, human epidermal growth factor receptor-2-negative estrogen receptor 1-mutant advanced or metastatic breast cancer.
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Celltrion building and skyline

Celltrion to buy Lilly’s cGMP plant for $330M, invest up to $1B

Sep. 23, 2025
By Marian (YoonJee) Chu
No Comments
Celltrion Inc. announced plans to acquire from Eli Lilly and Co. a Branchburg, N.J.-based biologics cGMP facility for $330 million up front, with plans to invest up to a total of ₩1.4 trillion (US$1 billion) in plant acquisition and expansion.
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