$GILD (Gilead Sciences Inc.)

$GILD {{ '2015-07-28T23:24:24+0000' | timeago}} • Webcast

$GILD 2Q15 Q&A: Matt of UBS asked for more perspective on product sales guidance, and Paul said outside of US, GILD has various dynamics going on. The company somewhat sees an early spike in volumes as people who are very sick and really need immediate treatment do get treated. GILD is also taking a conservative view of budget ceilings in Europe.

$GILD {{ '2017-09-15T13:21:02+0000' | timeago}} • Announcement

$GILD announced the pricing of senior unsecured notes in an aggregate principal amount of $3Bil, in an underwritten, registered public offering. The offering is expected to close September 21, 2017, subject to customary closing conditions. $GILD intends to use the net proceeds from the offering to finance a portion of the Kite acquisition.

$GILD {{ '2017-08-28T14:12:29+0000' | timeago}} • Announcement

$GILD agreed to acquire $KITE for $180 per share in cash, or approx. $11.9Bil in total. The deal is expected to close in 4Q17, and is expected to be neutral to earnings by year three and accretive thereafter. $GILD plans to finance the transaction with a combination of cash on hand, bank debt and senior unsecured notes.

$GILD {{ '2017-08-02T13:17:21+0000' | timeago}} • Announcement

$GILD announced that the US FDA has approved updated labeling for Epclusa, an all-oral, pan-genotypic, once-daily single tablet regimen for the treatment of adults with chronic hepatitis C virus (HCV) infection, to include use in patients co-infected with HIV.

$GILD {{ '2017-07-27T19:17:21+0000' | timeago}} • Webcast

$GILD stated that for Genvoya, it is starting to see performance trends similar to that of the US in other countries like Germany. The company is seeing good uptake in Spain and Italy. France has also done extraordinarily well in just four months to become the leading naïve and switch product.

$GILD {{ '2017-07-27T19:04:57+0000' | timeago}} • Webcast

For HCV, $GILD’s total revenues in the US were $1.9Bil in 2Q17, down 17% YoY and up 13% sequentially. The QoQ increase was primarily due to a change in inventory and the timing of patient starts. In Europe, total HCV revenue was $591MM, down 24% YoY and up 21% from 1Q17.

$GILD {{ '2017-07-27T19:00:11+0000' | timeago}} • Webcast

$GILD is seeing strong uptake of its TAF-based regimens in the US and Europe. In the US, total HIV and HBV revenues were $2.6Bil for 2Q17, up 19% YoY and up 10% sequentially. In Europe, total HIV and HBV revenues were $732MM, down 3% YoY and up 5% sequentially. The YoY decrease was driven by negative foreign exchange.

$GILD {{ '2017-07-27T18:32:52+0000' | timeago}} • Announcement

$GILD declared a cash dividend of $0.52 per share of common stock for 3Q17, payable on September 28, 2017, to stockholders of record on September 15, 2017.

$GILD {{ '2017-07-26T21:10:46+0000' | timeago}} • Infographic

$GILD Gilead Sciences Earnings AlphaGraphic: Q2 2017 Highlights

$GILD {{ '2017-07-26T20:37:51+0000' | timeago}} • Announcement

$GILD revised its FY17 guidance. The company now expects net product sales to be $24-25.5Bil in FY17. Non-HCV product sales are expected to be $15.5-16Bil while HCV product sales are expected to be $8.5-9.5Bil. Adjusted product gross margin is expected to be 86-88% in FY17.

$GILD {{ '2017-07-26T20:33:53+0000' | timeago}} • Announcement

$GILD's total product sales for 2Q17 were $7Bil compared to $7.7Bil for 2Q16. Product sales were $5Bil in the US, $1.4Bil in Europe and $665MM in other locations during 2Q17. Antiviral product sales were $6.4Bil and Other product sales were $607MM for 2Q17.

$GILD {{ '2017-07-26T20:29:32+0000' | timeago}} • Announcement

$GILD posted a slight decrease in 2Q17 results. Net income was $3.1Bil or $2.33 per share compared to $3.5Bil or $2.58 per share in 2Q16. Adjusted net income was $3.4Bil or $2.56 per share in 2Q17. Total revenues were $7.1Bil compared to $7.8Bil in the prior-year period.

$GILD {{ '2017-07-24T13:41:56+0000' | timeago}} • Announcement

$GILD announced results from two Phase 3 studies evaluating the efficacy and safety of a fixed-dose combination of bictegravir (BIC) and emtricitabine/tenofovir alafenamide (FTC/TAF) for the treatment of HIV-1 infection in treatment-naïve adults. This regimen has been well tolerated with low rates of discontinuations due to adverse events.

$GILD {{ '2017-07-18T20:14:00+0000' | timeago}} • Announcement

$GILD said the US FDA has approved Vosevi tablets, a single-tablet regimen for the re-treatment of chronic hepatitis C virus (HCV) infection in adults previously treated with or without an NS5A inhibitor-containing regimen. The approval is based on data from the Phase 3 POLARIS-1 and POLARIS-4 studies.

$GILD {{ '2017-07-13T13:10:29+0000' | timeago}} • Announcement

$GILD said its Marketing Authorization Application for an investigational, once-daily single tablet regimen containing bictegravir and emtricitabine/tenofovir alafenamide, formulations for treatment of HIV-1 infection in adults, has been fully validated. Currently, they are under evaluation by the European Medicines Agency.

$GILD {{ '2017-06-23T12:05:41+0000' | timeago}} • Announcement

$GILD said the Committee for Medicinal Products for Human Use (CHMP), the scientific committee of the European Medicines Agency(EMA), has adopted a positive opinion on its Marketing Authorization Application (MAA) for Vosevi for the treatment of chronic hepatitis C virus (HCV)-infected patients.

$GILD {{ '2017-06-12T15:03:28+0000' | timeago}} • Announcement

$GILD has submitted a New Drug Application to the FDA for an investigational, once-daily single tablet regimen for the treatment of HIV-1 infection in adults.

$GILD {{ '2017-05-30T14:13:41+0000' | timeago}} • Announcement

$GILD announced that four Phase 3 studies evaluating a fixed-dose combination of bictegravir (50mg) (BIC)  and emtricitabine/tenofovir alafenamide (200/25mg) (FTC/TAF) for the treatment of HIV-1 infection met their primary objectives of non-inferiority.

$GILD {{ '2017-05-05T19:17:07+0000' | timeago}} • Infographic

$GILD Gilead Sciences Earnings AlphaGraphics: Q1 2017 highlights

$GILD {{ '2017-05-02T21:57:30+0000' | timeago}} • Webcast

$GILD stated that the news about futility analysis is a rumor. The company clarified that it does not have an interim analysis planned in Phase III study. The study will be carried out for 48 weeks, $GILD said.

$GILD {{ '2017-05-02T21:45:49+0000' | timeago}} • Webcast

$GILD stated that about 55% of HIV sales is from public and about 45% is from the private in U.S. Of that 55%, 20% or so is from AIDS Drug Assistance Program (ADAP).

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