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Eli Lilly and Company

FDA issues complete response letter for donanemab

20 January 2023 | By Catherine Eckford (European Pharmaceutical Review)

A complete response letter for Eli Lilly's accelerated approval submission of donanemab for early Alzheimer's has been issued by the US Food and Drug Administration (FDA).

Lilly and EVA Pharma to aid affordable insulin access in lower income countries, Africa

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Lilly and EVA Pharma to aid affordable insulin access in Africa

15 December 2022 | By Catherine Eckford (European Pharmaceutical Review)

Insulin for at least one million diabetics in low- and middle-income countries, mainly in Africa, is the aim of Eli Lilly and EVA Pharmaceutical's new collaboration.

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Jardiance^® improves blood sugar control in type 2 diabetes

7 December 2022 | By Catherine Eckford (European Pharmaceutical Review)

A Phase III trial showed Jardiance® is the first SGLT2 inhibitor to significantly reduce average blood sugar in type 2 diabetics aged 10-17 compared to placebo.

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Empagliflozin reduces risk of chronic kidney disease progression

7 November 2022 | By Catherine Eckford (European Pharmaceutical Review)

A major trial evaluating Boehringer Ingelheim’s Jardiance®, showed it reduced the risk of cardiovascular death and chronic kidney disease progression by 28 percent.

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Lilly will acquire Akouos to accelerate hearing loss therapies

19 October 2022 | By Catherine Eckford (European Pharmaceutical Review)

Eli Lilly and Company’s $610 million acquisition of Akouos will fast-track gene therapies that restore, improve and preserve hearing for patients worldwide.

3D illustration of Medicine capsule showing its active ingredients

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HPAPI market to value $27bn by 2025

8 June 2022 | By Hannah Balfour (European Pharmaceutical Review)

Driven by oncology drug demand, the highly potent active pharmaceutical ingredients (HPAPIs) market is anticipated to grow by $7bn in three years.

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Lilly to build two new US manufacturing sites

31 May 2022 | By Hannah Balfour (European Pharmaceutical Review)

Eli Lilly and Company announces plans to establish two new manufacturing facilities in Indiana USA worth $2.1 billion.

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Eli Lilly shares impressive hair regrowth results with Olumiant^® for alopecia

30 March 2022 | By Mandy Parrett (European Pharmaceutical Review)

The results of Eli Lilly and Company’s double-blind, placebo-controlled Phase III trials for Olumiant® are encouraging for patients suffering with alopecia.

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Empagliflozin trial halted after successful outcome in chronic kidney disease

21 March 2022 | By European Pharmaceutical Review

An early halt has been called to a major kidney drug trial following positive results for patients with chronic kidney disease (CKD).

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Empagliflozin benefits adults hospitalised for acute heart failure, shows study

4 March 2022 | By European Pharmaceutical Review

Phase III trial shows that adults hospitalised for acute heart failure were 36 percent more likely to experience a clinical benefit if initiated on empagliflozin.

blue and clear capsule with a silver DNA stand inside - idea of gene therapy

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Lilly to create $700mn Institute for Genetic Medicine

23 February 2022 | By Hannah Balfour (European Pharmaceutical Review)

Investing $700mn to establish a new site, Eli Lilly plans to fuel the development of genetic medicines through the company’s new Institute for Genetic Medicine.

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Lilly to build new $1bn manufacturing facility in US

31 January 2022 | By Hannah Balfour (European Pharmaceutical Review)

The new North Carolinian site will increase parenteral and device manufacturing capacity and create 600 new jobs.

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ProQR and Lilly collaborate to develop RNA therapeutic

9 September 2021 | By Anna Begley (European Pharmaceutical Review)

ProQR and Lilly announced a collaboration to combat genetic disorders in the liver and nervous system using Axiomer® RNA editing platform.

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Lilly to collaborate with Lycia on novel protein degraders

26 August 2021 | By Hannah Balfour (European Pharmaceutical Review)

The collaborators will use Lycia’s lysosomal targeting chimera (LYTAC) protein degradation platform to develop therapies for five targets across Lilly’s therapeutic areas of focus.

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FDA approves Jardiance^® for heart failure with reduced ejection fraction

19 August 2021 | By Anna Begley (European Pharmaceutical Review)

The FDA have approved Lilly’s Jardiance (empagliflozin) to treat adults living with heart failure with reduced ejection fraction.

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Eli Lilly and Company