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Last SFr.80.60 CHF
Change Today -1.00 / -1.23%
Volume 0.0
LLY On Other Exchanges
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As of 11:43 AM 10/8/15 All times are local (Market data is delayed by at least 15 minutes).

eli lilly & co (LLY) Snapshot

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52 Week High
07/21/15 - SFr.88.00
52 Week Low
10/16/14 - SFr.59.10
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Current Stock Chart for ELI LILLY & CO (LLY)

eli lilly & co (LLY) Details

Eli Lilly and Company discovers, develops, manufactures, and sells pharmaceutical products worldwide. It operates through two segments, Human Pharmaceutical Products and Animal Health Products. The company offers endocrinology products to treat diabetes; osteoporosis in postmenopausal women and men; human growth hormone deficiency and pediatric growth conditions; and testosterone deficiency. It also provides neuroscience products for the treatment of major depressive disorders, diabetic peripheral neuropathic pain, anxiety disorders, fibromyalgia, and chronic musculoskeletal pain; schizophrenia; attention-deficit hyperactivity disorders; depressive, obsessive-compulsive, bulimia nervosa, and panic disorders; and positron emission tomography imaging of beta-amyloid neurotic plaques in adult brains. In addition, the company offers products for the treatment of non-small cell lung, colorectal, head and neck, pancreatic, metastatic breast, ovarian, bladder, and metastatic gastric cancers, as well as malignant pleural mesothelioma; and cardiovascular products for the treatment of erectile dysfunction and benign prostatic hyperplasia, thrombotic cardiovascular events, and cardiac ischemic complications. Further, it provides animal health products, such as cattle feed additives; protein supplements for cows; leanness and performance enhancers for swine, cattle, and poultry; antibiotics to treat respiratory and other diseases in cattle, swine, and poultry; anticoccidial agents for poultry; and chewable tablets that kill fleas and prevent flea infestations, heartworm diseases, roundworm diseases, hookworm diseases, and whipworm diseases. Additionally, the company offers products to treat chronic manifestations of atopic dermatitis and congestive heart failure in dogs; chronic allergic dermatitis and kidney diseases in cats. It has collaboration agreement with ZP Opco, Inc. Eli Lilly and Company was founded in 1876 and is headquartered in Indianapolis, Indiana.

39,135 Employees
Last Reported Date: 02/19/15
Founded in 1876

eli lilly & co (LLY) Top Compensated Officers

Chairman, Chief Executive Officer and Preside...
Total Annual Compensation: $1.5M
Chief Financial Officer, Executive Vice Presi...
Total Annual Compensation: $1.0M
Executive Vice President of Science & Technol...
Total Annual Compensation: $1.0M
Senior Vice President and President of Lilly ...
Total Annual Compensation: $682.9K
General Counsel and Senior Vice President
Total Annual Compensation: $765.0K
Compensation as of Fiscal Year 2014.

eli lilly & co (LLY) Key Developments

Eli Lilly and Company and Avid Radiopharmaceuticals, Inc. Announce Financial Commitment and Continued Scientific Partnership

Eli Lilly and Company and Avid Radiopharmaceuticals, Inc. announced financial commitment and continued scientific partnership to support the recently established Imaging Dementia 'Evidence for Amyloid Scanning (IDEAS) Study'. The IDEAS Study will assess the clinical usefulness and value in using an amyloid brain positron emission tomography (PET) scan in certain situations when evaluating Alzheimer's disease (AD) and other dementias. Amyvid™ (Florbetapir F-18 Injection), Lilly's FDA-approved radioactive PET diagnostic agent for the estimation of beta-amyloid neuritic plaque density in the brain, will be one diagnostic agent available for use in the study. Manufactured in and distributed from 30 radiopharmacy facilities throughout the United States, Amyvid is currently supplied to a robust network of PET imaging sites by Siemens' PETNET Solutions and Cardinal Health. Amyvid for intravenous use is supplied in 10 mL, 30 mL, or 50 mL multidose vials containing 500-1900 MBq/mL Florbetapir F-18.

Zosano Dissolves Licensing Partnership with Eli Lilly for ZP-PTH

Zosano Pharma (US) has announced it will stop developing the daily version of its ZP-PTH candidate treatment for severe osteoporosis and instead resume development of the weekly version. The company said its decision was prompted by feedback from Japanese regulatory authorities that they would require additional studies that would be likely to delay commercialisation in Japan by about a year. Zosano's licensing partnership with Eli Lilly (US) for ZP-PTH has therefore been dissolved. Zosano has discontinued its development of daily ZP-PTH despite reportedly receiving positive feedback from the US FDA and it had been on course to initiate a Phase III programme in the United States. In light of the feedback from the Japanese authorities, however, Zosano believes its resources would be more prudently deployed by focusing on weekly ZP-PTH, for which it is planning to initiate a Phase II trial in the first half of 2016. Zosano had entered into its partnership with Lilly in late 2014.

Adocia and Eli Lilly and Company Initiate New Phase 1b Study of Repeat Administration of Ultra-Rapid BioChaperone Lispro in Patients with Type 2 Diabetes

Adocia and Eli Lilly and Company announced the initiation of a Phase 1b clinical trial evaluating BioChaperone Lispro, an ultra-rapid formulation of insulin lispro licensed to Lilly. This formulation uses Adocia's proprietary technology, BioChaperone, to accelerate insulin absorption. This study, under the Adocia-Lilly partnership, aims to measure the effect of BioChaperone Lispro injected at mealtime on post-meal glycemic control in type 2 diabetes patients compared to that of Humalog® (insulin lispror DNA origin) over the same two-week period. Commercialized fast-acting insulin analogs are usually injected before the meal. An ultra-rapid insulin aims to allow injection at the time of the meal, or even after the start of a meal, with the goal of reducing the magnitude of glycemic excursions. The first clinical study conducted by the two companies demonstrated that BioChaperone Lispro was associated with a 61% reduction in post-prandial glucose excursions over the first two hours post-meal compared to Humalog. This new clinical study is designed to document the potential benefit of BioChaperone Lispro in patients with type 2 diabetes, a population representing about 90% of people living with diabetes. In this crossover, randomized, double-blind study, 50 subjects with type 2 diabetes will receive multiple daily doses of BioChaperone Lispro and multiple daily doses of Humalog over two periods of 14 days each. The main objective of this study is to compare the post-meal glycemic control obtained after the injection of either BioChaperone Lispro or Humalog immediately before the meal. The pharmacokinetic profiles of both products will also be monitored. This study will be sponsored by Adocia, and performed by Profil Neuss in Germany.


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Valuation LLY Industry Range
Price/Earnings 44.9x
Price/Sales 4.7x
Price/Book 6.3x
Price/Cash Flow 46.6x
TEV/Sales 4.3x

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