$REGN (Regeneron Pharmaceuticals, Inc.)

$REGN {{ '2017-08-03T14:59:22+0000' | timeago}} • Webcast

The US sales of $REGN’s flagship macular degeneration drug EYLEA rose 10% YoY in the first half of 2017, driven by higher demand and increased market share. Regeneron expects to fully utilize the $130MM annual funding from its collaborator Sanofi, under an antibody discovery agreement, by the end of the third quarter.

$REGN {{ '2017-10-16T14:56:28+0000' | timeago}} • Announcement

$REGN and $SNY announced positive results from a Phase 2 study of dupilumab in adults with active moderateto-severe eosinophilic esophagitis (a condition that causes swallowing difficulty). The study showed that patients who received dupilumab weekly reported a significant improvement in the ability to swallow versus placebo.

$REGN {{ '2017-10-16T13:04:52+0000' | timeago}} • Announcement

$REGN and Sanofi announced positive results from a Phase 2 investigational study of dupilumab in adults with active moderate-to-severe eosinophilic esophagitis. Eosinophilic esophagitis is a chronic, allergic inflammatory disease that damages the esophagus and prevents it from working properly, leading to difficulties swallowing and food impaction.

$REGN {{ '2017-10-05T17:28:07+0000' | timeago}} • Announcement

Sanofi and $REGN said the U.S. Court of Appeals for the Federal Circuit has ordered new trial and vacated permanent injunction in the dispute concerning $AMGN's asserted patent claims for antibodies targeting PCSK9. This ruling means that Sanofi and $REGN will continue marketing, selling and manufacturing Praluent (alirocumab) injection in the U.S.

$REGN {{ '2017-10-02T12:04:30+0000' | timeago}} • Announcement

Pharma company $REGN has entered into collaborations with the Biomedical Advanced Research & Development Authority to develop  treatments for infectious diseases. The first collaboration is focused on development of antibodies targeting up to 10 pathogens, while the second builds on a prior agreement to develop a potential therapy for Ebola virus.

$REGN {{ '2017-09-28T12:24:36+0000' | timeago}} • Announcement

$REGN and $SNY have announced that the European Commission has granted marketing authorization for DUPIXENT (dupilumab), for use in adults with moderate-to-severe atopic dermatitis (AD) who are candidates for systemic therapy. AD, a form of eczema, is a chronic inflammatory disease with symptoms often appearing as a rash on the skin.

$REGN {{ '2017-09-18T10:59:56+0000' | timeago}} • Announcement

Pharma company $REGN and healthcare firm $SNY said a study showed that Dupixent, which is indicated for the treatment of atopic dermatitis, significantly improved overall disease severity. It also met the primary end point - the proportion of patients that achieved a 75% or greater improvement at 16 weeks from baseline.

$REGN {{ '2017-09-11T11:11:52+0000' | timeago}} • Announcement

$REGN and Sanofi announced positive dupilumab topline results from phase 3 trial in uncontrolled persistent asthma. The investigational dupilumab lowered severe asthma attacks and improved lung function. The companies plan to submit a Supplemental Biologics License Application (sBLA) to the U.S. FDA by the end of this year.

$REGN {{ '2017-08-14T13:55:04+0000' | timeago}} • Announcement

$REGN has announced that it would discontinue developing its drug to prevent respiratory syncytial virus (RSV) infections in infants. Its Phase 3 study evaluating suptavumab, an antibody to RSV, did not meet its primary endpoint of preventing the infection following which the company planned to stop further clinical development of this antibody.

$REGN {{ '2017-08-03T14:59:22+0000' | timeago}} • Webcast

The US sales of $REGN’s flagship macular degeneration drug EYLEA rose 10% YoY in the first half of 2017, driven by higher demand and increased market share. Regeneron expects to fully utilize the $130MM annual funding from its collaborator Sanofi, under an antibody discovery agreement, by the end of the third quarter.

$REGN {{ '2017-08-03T14:30:54+0000' | timeago}} • Webcast

$REGN said its arthritis drug Kevzara received approval from the US FDA and the European Commission in 2Q17. In the second half of this year, topline data from phase-2 studies on wet age related macular degeneration and diabetic macular edema are expected to be published. Results from study on a cardiovascular drug will be released in early 2018.

$REGN {{ '2017-08-03T12:12:28+0000' | timeago}} • Announcement

$REGN raised sales growth forecast for FY17 to 10% from the earlier outlook of single-digit increase. The company anticipates non-GAAP R&D expenses between $925MM and $965MM. The guidance of non-GAAP selling, general and administrative expenses has been raised to the range of $1.12-$1.16Bil. Regeneron sees effective tax rate of 27-31% for the year.

$REGN {{ '2017-08-03T11:54:57+0000' | timeago}} • Announcement

Earnings of pharmaceuticals company $REGN nearly doubled to $388MM in 2Q17 as strong sales of its leading products, including the EYLEA injection, lifted revenues by 21% to $1.47Bil. EPS grew 48%YoY to $3.34, while non-GAAP earnings advanced to $4.17 per share. The higher revenues resulted in an 88% gain in operating income.

$REGN {{ '2017-07-21T15:50:38+0000' | timeago}} • Announcement

$REGN and $SNY announced that the European Medicine Agency's Committee for Medicinal Products for Human Use has given a positive opinion for the marketing authorization of Dupixent (dupilumab), recommending its approval in Europe for use in adults with moderate-to-severe atopic dermatitis who are candidates for systemic therapy.

$REGN {{ '2017-06-22T14:02:42+0000' | timeago}} • Announcement

$REGN provided details of the royalty it receives on any sales of canakinumab (ACZ885). $REGN received a royalty on worldwide net sales of canakinumab; the royalty rate starts at 4% and reaches 15% when canakinumab annual sales exceed $1.5Bil.

$REGN {{ '2017-06-12T10:58:03+0000' | timeago}} • Announcement

$REGN and $SNY announced positive results from two Phase 3b/4 ODYSSEY-DM trials in patients with diabetes. In the studies, Praluent, when administered on top of maximally tolerated doses of statins, significantly reduced low-density lipoprotein cholesterol, the primary endpoint of the study.

$REGN {{ '2017-06-05T12:01:45+0000' | timeago}} • Announcement

$REGN and Sanofi announced positive preliminary results with investigational REGN2810 in patients with advanced cutaneous squamous cell carcinoma (CSCC). CSCC is the second most common type of skin cancer in the U.S.

$REGN {{ '2017-05-23T12:31:01+0000' | timeago}} • Announcement

$REGN said the U.S. Food and Drug Administration (FDA) approval of Kevzara (sarilumab) for the treatment of adult patients with moderately to severely active rheumatoid arthritis (RA) who have had an inadequate response to one or more disease modifying antirheumatic drugs, such as methotrexate (MTX).

$REGN {{ '2017-05-08T12:57:32+0000' | timeago}} • Announcement

$REGN and SillaJen, Inc. announced a new clinical and supply agreement for a Phase 1b dose-escalation study in renal cell carcinoma. Under the terms of the agreement, the trial will be solely conducted and funded by SillaJen based upon a mutually developed study design and $REGN will provide REGN2810.

$REGN {{ '2017-05-08T12:56:18+0000' | timeago}} • Announcement

$REGN and SillaJen, Inc. announced a new clinical and supply agreement for a Phase 1b dose-escalation study in renal cell carcinoma. The open-label trial is expected to begin later this year, and is designed to evaulate the safety and efficacy of REGN2810 in combination with Pexa-Vec compared to treatment with REGN2810 as monotherapy.

$REGN {{ '2017-05-08T12:38:36+0000' | timeago}} • Announcement

$REGN and $INO announced a clinical study agreement for a phase 1b/2a immuno-oncology trial for glioblastoma combination therapy. Glioblastoma is the most common and aggressive type of brain cancer. The open-label trial is expected to begin later this year.

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