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ABBV names executive to oversee AGN’s medical aesthetics business following merger:
https://finance.yahoo.com/news/abbvie-announces-leadership-team-creation-130000368.html
AbbVie's JAK Inhibitor Rinvoq Receives Approval for RA in EU
“AbbVie Inc. ABBV announced that the European Commission has granted approval to its JAK inhibitor, Rinvoq (upadacitinib) for the treatment of moderate-to-severe rheumatoid arthritis (“RA”) in patients who experience inadequate response or are intolerant to disease-modifying anti-rheumatic drugs (DMARDs). The drug is approved as a monotherapy or in combination with methotrexate in this patient population.
Please note that the JAK inhibitor had received approval for a similar indication in the United States in August and the early uptake trends of the drug have been encouraging.Rinvoq has generated sales of $14 million in the third quarter since its approval.
Shares of AbbVie have gained 14% in the past six months compared with the industry’s increase of 6%.
The approval for Rinvoq in Europe was based on encouraging data from the phase III SELECT program, which evaluated more than 4000 patients across five phase III studies on RA. In all studies, the drug met every primary and secondary endpoint. Data from the studies under the SELECT program demonstrated that Rinvoq alone or in combination with conventional synthetic DMARDs improved rates of low disease activity and clinical remission in RA patients compared to placebo, MTX or AbbVie’s blockbuster inflammatory drug, Humira (adalimumab).
Humira is the primary revenue generator for AbbVie with global sales of more than $14 billion in the first nine months of 2019. However, the drug’s sales declined significantly in Europe due to the launch of several biosimilars last year from companies including Amgen AMGN, Biogen BIIB and Novartis NVS. Moreover, the drug is set to lose patent protection in the United States, beginning 2023. A similar decline in U.S. sales for the drug will significantly dent AbbVie’s revenues going forward.
We expect Rinvoq and AbbVie’s another new inflammation drug, Skyrizi, to partially offset lost sales for Humira over the long term. However, Humira is approved for 10 different inflammatory indications. AbbVie’s efforts to expand labels of Skyrizi and Rinvoq will further reduce the impact of patent loss for Humira on its revenues, if successful.
In a separate event, the company has reportedly entered into an agreement with the pan-Canadian Pharmaceutical Alliance for the commercialization of Venclexta in combination with J&J’s Rituxan (rituximab) as a treatment for chronic lymphocytic leukemia in second or later-line setting.”
https://finance.yahoo.com/news/abbvies-jak-inhibitor-rinvoq-receives-150103062.html
$ABBV short squeeze signal Abbvie Inc Nyse Abbv Short Squeeze
Looks like we got some good news on that front
ABBV sells $30B of bonds to fund AGN acquisition: #msg-152249872.
News: $ABBV This Terrific High-Yield Dividend Stock Just Got Even Better
What's better than a stock that pays great dividends? A stock that pays great dividends and keeps hiking those dividends. That's exactly what AbbVie (NYSE: ABBV) has done since being spun off from Abbott Labs in 2013, raising its dividend every year. If you count the period when AbbVie ...
Read the whole news ABBV - This Terrific High-Yield Dividend Stock Just Got Even Better
News: $ABBV 2 Biotech Stocks Fighting Alzheimer's Disease to Own Now
The Alzheimer's community got a boost at the end of October when Biogen (NASDAQ: BIIB) announced it would file for approval from the U.S. Food and Drug Administration for aducanumab, its Alzheimer's disease drug. This caught patients and investors off guard since Biogen scrapped the pro...
In case you are interested ABBV - 2 Biotech Stocks Fighting Alzheimer's Disease to Own Now
Rinvoq phase-3 hits in psoriatic arthritis:
https://finance.yahoo.com/news/rinvoq-upadacitinib-meets-primary-ranked-124500628.html
Allergan Shareholders Approve Proposed Acquisition by AbbVie
https://www.prnewswire.com/news-releases/allergan-shareholders-approve-proposed-acquisition-by-abbvie-300937774.html
AbbVie-Allergan Merger - Don't Worry About Debt, AbbVie Is Still A Buy
https://seekingalpha.com/article/4295290-abbvie-allergan-merger-worry-debt-abbvie-still-buy
I thought about dumping my ABBV yesterday, but then remembered how nice the dividend is. Maybe I'll wait for pitiful pete to comment then do the opposite.
Give this a listen and some thought:
Highlight: “For the last 4 years, we’ve been struggling with this drug pricing issue and payers are pushing back,” says @bradloncar. “This industry has fundamentally changed and it’s really impacted the growth of biotech as a whole.” But there are bright spots, he adds.
Highlight: “For the last 4 years, we’ve been struggling with this drug pricing issue and payers are pushing back,” says @bradloncar. “This industry has fundamentally changed and it’s really impacted the growth of biotech as a whole.” But there are bright spots, he adds. pic.twitter.com/6cYk8Frtv0
— Yahoo Finance (@YahooFinance) September 30, 2019
Management and the BOD`s have a lot to concern themselves with just getting the buyout approved, doubt we`ll get any uptick of dividend, but you never know.
Hopefully that will lead to an increase in dividends. :)
06:38am 09/26/2019
AbbVie, Allergan rating change at Citi
Citi upgrades AbbVie to Buy, sees 'significant' value from Allergan deal. Citi analyst Andrew Baum upgraded AbbVie to Buy from Neutral and raised his price target for the shares to $90 from $87. The analyst believes AbbVie will "extract significant shareholder value" from Allergan's (AGN) franchises given its "strong commercial focus and patient/physician centricity." Further, within AbbVie's organic portfolio, Baum continues to think the market underappreciates the revenue potential.
AbbVie Is One Of The Best High-Yield Stocks You Can Buy Right Now
Sep. 23, 2019 8:15 AM
https://seekingalpha.com/article/4292892-abbvie-one-best-high-yield-stocks-can-buy-right-now
Jim Cramer assesses recent acquisitions in AbbVie and Bristol-Myers
Thursday, 19 Sep 2019 | 5:00 PM PT
Jim Cramer breaks down large acquisitions that AbbVie and Bristol-Myers recently made and explains why he's recommending AbbVie as a buy.
Their acquisition of Allergan will create a new company churning out $20 billion in free cash flow a year, plus a much needed pipeline.
https://www.cnbc.com/video/2019/09/20/jim-cramer-assesses-recent-acquisitions-in-abbvie-and-bristol-myers.html
Dew are you long ABBV?
I don't think so. AGN's opioid-litigation exposure is pretty small in the overall scheme of things.
Could ABBV dump AGN if opioid damages become excessive?
ABBV formally dumps Rova-T program after another phase-3 failure:
https://finance.yahoo.com/news/abbvie-discontinues-rovalpituzumab-tesirine-rova-124500700.html
That’s what I’m hoping for when I bought in recently. One concern is them socialist on the left wanting to drastically change the medical tho
ABBV is a screaming buy.
FDA approves ABBV’s Rinvoq (upadacitinib) for RA:
https://finance.yahoo.com/news/abbvie-receives-fda-approval-rinvoq-164300881.html
https://finance.yahoo.com/news/1-fda-approves-abbvies-rheumatoid-164927079.html
Rinvoq is an oral JAK inhibitor; it is one of the drugs ABBV is counting on to make up the slack as Humira sales decline from the uptake of biosimilars.
The US list price of Rinvoq is ~$59K per annum, which is slightly less than Humira.
$ABBV AbbVie Submits New Drug Application to US FDA for Investigational Elagolix for Management of Heavy Menstrual Bleeding Associa...
Source: PR Newswire (US)
NORTH CHICAGO, Ill., Aug. 5, 2019 /PRNewswire/ -- AbbVie (NYSE: ABBV), a research-based global biopharmaceutical company, in cooperation with Neurocrine Biosciences, Inc. (NASDAQ: NBIX), today announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for elagolix, an investigational, oral gonadotropin-releasing hormone (GnRH) antagonist, for the management of heavy menstrual bleeding (HMB) associated with uterine fibroids in women.
Uterine fibroids are non-cancerous, hormonally-responsive muscle tissue tumors of the uterus.1 They can affect up to 70% of Caucasian women and up to 80% of African American women by age 50.2 Fibroids can be asymptomatic but, in some women, fibroids can cause symptoms, such as heavy menstrual bleeding (HMB), vaginal bleeding at times other than menstruation, and anemia.1,3
"This submission brings us closer to our goal of improving care for women who continue to struggle with the often disruptive effects of uterine fibroids," said Michael Severino, M.D., vice chairman and president, AbbVie. "If approved, this combination has the potential to offer women and their healthcare providers an additional oral medical treatment option."
The NDA is supported by data from the elagolix Phase 3 uterine fibroid program, which evaluated nearly 800 premenopausal women with HMB associated with uterine fibroids in two pivotal studies (ELARIS UF-I and ELARIS UF-II) at approximately 100 sites in the U.S. and Canada. The replicate studies evaluated the safety, tolerability and efficacy of elagolix alone (300 mg twice daily, or BID) and in combination with low-dose hormone (add-back) therapy (estradiol 1.0 mg/norethindrone acetate 0.5 mg) in women with uterine fibroids for six months. An extension study permitted women to be treated for an additional six months.
The primary endpoint assessed the reduction in HMB compared to placebo as measured by the alkaline hematin method, an objective measurement of total menstrual blood loss (MBL) based on quantification of menstrual blood collected on sanitary products. In both studies, elagolix in combination with add back therapy met the primary endpoint. The most frequent adverse events reported (≥ 5 percent) were hot flush, night sweats, nausea, headache and fatigue.4
Top-line results from these clinical studies were previously announced at the 47th American Association of Gynecologic Laparoscopists (AAGL) Global Congress on Minimally Invasive Gynecology. Detailed results from the Phase 3 program will be published in a peer-reviewed medical journal later this year.
Elagolix for the management of HMB associated with uterine fibroids is investigational and its safety and efficacy have not been evaluated by any regulatory authorities.
About Uterine Fibroids
Uterine fibroids (also called leiomyomas or myomas) are non-cancerous, hormonally-responsive muscle tissue tumors of the uterus.1 Fibroids are the most common type of abnormal growth in a woman's pelvis1 and can affect up to 70% of Caucasian women and up to 80% of African American women by age 50.2 Fibroids can range in size, shape, number and location.1,3 Fibroids can be asymptomatic but, in some women, they can cause symptoms such as heavy menstrual bleeding (HMB), vaginal bleeding at times other than menstruation, anemia, and other symptoms related to women's health.1,3 Treatment options for uterine fibroids include surgery (hysterectomy, myomectomy), endometrial ablation, uterine artery embolization, magnetic resonance imaging (MRI)-guided ultrasound and medical management with treatments such as oral contraceptives, progestins, selective progesterone receptor modulators, and gonadotropin-releasing hormone (GnRH) agonists.1,5
About Elagolix
Elagolix is an orally-administered, nonpeptide, small molecule gonadotropin-releasing hormone (GnRH) receptor antagonist that inhibits endogenous GnRH signaling by binding competitively to GnRH receptors in the pituitary gland.6 Administration results in dose-dependent suppression of luteinizing hormone (LH) and follicle-stimulating hormone (FSH), leading to decreased blood concentrations of the ovarian sex hormones estradiol and progesterone.6 Elagolix is currently being investigated in diseases that are mediated by ovarian sex hormones, such as uterine fibroids and polycystic ovary syndrome.
About AbbVie
AbbVie is a global, research and development-based biopharmaceutical company committed to developing innovative advanced therapies for some of the world's most complex and critical conditions. The company's mission is to use its expertise, dedicated people and unique approach to innovation to markedly improve treatments across four primary therapeutic areas: immunology, oncology, virology and neuroscience. In more than 75 countries, AbbVie employees are working every day to advance health solutions for people around the world. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, LinkedIn or Instagram.
Forward-Looking Statements
Some statements in this news release are, or may be considered, forward-looking statements for purposes of the Private Securities Litigation Reform Act of 1995. The words "believe," "expect," "anticipate," "project" and similar expressions, among others, generally identify forward-looking statements. AbbVie cautions that these forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially from those indicated in the forward-looking statements. Such risks and uncertainties include, but are not limited to, competition from other products, challenges to intellectual property, difficulties inherent in the research and development process, adverse litigation or government action, and changes to laws and regulations applicable to our industry. Additional information about the economic, competitive, governmental, technological and other factors that may affect AbbVie's operations is set forth in Item 1A, "Risk Factors," of AbbVie's 2018 Annual Report on Form 10-K, which has been filed with the Securities and Exchange Commission. AbbVie undertakes no obligation to release publicly any revisions to forward-looking statements as a result of subsequent events or developments, except as required by law.
1 De La Cruz MS, Buchanan EM. Uterine Fibroids: Diagnosis and Treatment. Am Fam Physician. 2017 Jan 15;95(2):100-107.
2 Baird DD, Dunson DB, Hill MC, Cousins D, Schectman JM. High cumulative incidence of uterine leiomyoma in black and white women: ultrasound evidence. Am J Obstet Gynecol. 2013;188:100-107.
3 The American College of Obstetricians and Gynecologists: FAQ Uterine Fibroids. http://www.acog.org/-/media/For-Patients/faq074.pdf?dmc=1&ts=20170329T1658263942. Accessed May 15, 2019.
4 Data on File at AbbVie, ABVRRTI67252.
5 Alternatives to hysterectomy in the management of leiomyomas. ACOG Practice Bulletin No. 96. American College of Obstetricians and Gynecologist. Obstet Gynecol 2008; 112:387-400.
6 Ng J, et al. Dose-Dependent Suppression of Gonadotropins and Ovarian Hormones by Elagolix in Healthy Premenopausal Women. J Clin Endocrinol Metab. 2017;102(5):1683-1691
Cision View original content:http://www.prnewswire.com/news-releases/abbvie-submits-new-drug-application-to-us-fda-for-investigational-elagolix-for-management-of-heavy-menstrual-bleeding-associated-with-uterine-fibroids-in-women-300896046.html
SOURCE AbbVie
Copyright 2019 PR Newswire
Could be a good long term growth and dividend play at these levels.
$ABBV AbbVie's MAVIRET™ (glecaprevir/pibrentasvir) Approved by European Commission to Shorten Treatment Duration to Eight Weeks f...
Source: PR Newswire (US)
- MAVIRET™ is now available as a shorter, 8-week, once-daily option for treatment-naïve, compensated cirrhotic, chronic hepatitis C (HCV) patients with genotype (GT)1, 2, 4, 5 and 6
- Marketing authorization is supported by 97.9 percent cure* rate across this group of patients with no reported virologic failures1
- Analysis evaluating MAVIRET as an 8-week, once-daily treatment option for treatment-naïve, compensated cirrhotic, GT3 HCV patients is ongoing
NORTH CHICAGO, Illinois, Aug. 2, 2019 /PRNewswire/ -- AbbVie (NYSE: ABBV), a research-based global biopharmaceutical company, today announced that the European Commission has granted marketing authorization for MAVIRET™ (glecaprevir/pibrentasvir) to shorten once-daily treatment duration from 12 to 8 weeks in treatment-naïve, compensated cirrhotic, chronic hepatitis C (HCV) patients with genotype (GT)1, 2, 4, 5, and 6 infection. An analysis from the same clinical trial evaluating MAVIRET as an 8-week, once-daily treatment option for treatment-naïve, compensated cirrhotic, GT3 HCV patients is ongoing. MAVIRET is also currently approved as an 8-week, pan-genotypic (GT1-6) treatment for treatment-naïve patients without cirrhosis.2**
"MAVIRET has already had a significant impact on the lives of hundreds of thousands of people affected by chronic HCV, and with this approval, we are one step closer to providing more HCV patients with an option to treat their chronic disease with a once-daily, 8-week regimen," said Janet Hammond M.D., vice president, general medicine and virology therapeutic area, AbbVie.
The marketing authorization is supported by data from the ongoing Phase 3b EXPEDITION-8 study, which showed that with 8 weeks of MAVIRET, 97.9 percent (n=274/280) of GT1, 2, 4, 5 and 6 patients achieved a sustained virologic response 12 weeks after treatment (SVR12) (ITT).1 To date, no virologic failures have been reported in these patients and no patients have discontinued treatment due to adverse events.1 Adverse events (frequency >5%) reported in the study include pruritus (9.6%), fatigue (8.6%), headache (8.2%) and nausea (6.4%).1 Six serious adverse events (2%) have occurred during the study, none of which were deemed to be related to glecaprevir/pibrentasvir.1 No new safety signals were identified in this study.1 These data were presented as a late-breaking, oral presentation at The Liver Meeting® 2018 organized by the American Association for the Study of Liver Diseases (AASLD) in San Francisco, California.
The ongoing Phase 3b EXPEDITION-8 study is evaluating the safety and efficacy of MAVIRET in treatment-naïve chronic HCV patients with compensated cirrhosis across all major genotypes (GT1-6).1 The results have been reported for GT1, 2, 4, 5, and 6 (n=280) patients. Enrollment and treatment of the GT3 patient population was completed later, therefore the analysis of this population is ongoing.
"There are still a significant number of HCV patients with varied patient and viral characteristics who are in need of options," said Stefan Zeuzem, M.D., chief of the department of medicine at the J.W. Goethe University Hospital in Frankfurt, Germany. "We are working hard to help support achieving the World Health Organization's goal of eliminating HCV by 2030 and having additional patient populations eligible for shorter-term, 8-week treatment options could help bring us closer to that goal."
About the EXPEDITION-8 Study1
EXPEDITION-8 is an ongoing non-randomized, single arm, open-label, multicenter Phase 3b study evaluating the safety and efficacy of glecaprevir/pibrentasvir in treatment-naïve GT1-6 chronic HCV patients with compensated cirrhosis. Analysis of the GT3 patient population is ongoing.
The primary efficacy endpoints are the SVR12 rates in patients with GT1, 2, 4, 5, and 6 in a per-protocol (PP) and intent-to-treat (ITT) population versus respective historical SVR12 rates based on the efficacy of MAVIRET for 12 weeks in treatment-naïve patients with compensated cirrhosis. The SVR12 rates were 97.9 percent (n=274/280) and 100 percent (n=273/273) in the ITT and PP populations, respectively. From the 280 patients with GT1, 2, 4, 5 or 6 enrolled, seven were excluded from the SVR12 per-protocol analysis (n=273); five patients were lost to follow up, and two patients received less than 8 weeks of treatment (one of these two patients achieved SVR12). The key secondary efficacy endpoints are the percentages of GT1, 2, 3, 4, 5, and 6 patients achieving SVR12 in a PP and ITT population.
About MAVIRET™ (glecaprevir/pibrentasvir)
MAVIRET® is approved in the European Union for the treatment of chronic hepatitis C virus (HCV) infection in adults and adolescents 12 to <18 years old across all major genotypes (GT1-6). MAVIRET is a pan-genotypic, once-daily, ribavirin-free treatment that combines glecaprevir (100mg), an NS3/4A protease inhibitor, and pibrentasvir (40mg), an NS5A inhibitor, dosed once-daily as three oral tablets.
Maviret is an 8-week, pan-genotypic option (GT1-6) for patients who are new to treatment and without cirrhosis and for GT1, 2, 4, 5 and 6 patients who are new to treatment with compensated cirrhosis. The recommended duration of therapy for treatment-naive, compensated cirrhotic GT3 HCV patients is 12 weeks. MAVIRET is also approved as a treatment for patients with specific treatment challenges, including those with compensated cirrhosis across all major genotypes, and those who previously had limited treatment options, such as patients with severe chronic kidney disease (CKD) or those with genotype 3 chronic HCV infection. MAVIRET is a pan-genotypic treatment approved for use in patients across all stages of CKD. MAVIRET is contraindicated in patients with severe hepatic impairment (Child-Pugh C) and is not recommended in patients with moderate hepatic impairment (Child-Pugh B).2
Glecaprevir (GLE) was discovered during the ongoing collaboration between AbbVie and Enanta Pharmaceuticals (NASDAQ: ENTA) for HCV protease inhibitors and regimens that include protease inhibitors.
EU Indication
MAVIRET is indicated for the treatment of chronic hepatitis C virus (HCV) infection in adults and adolescents 12 to <18 years old.
Important EU Safety Information
Contraindications:
MAVIRET is contraindicated in patients with severe hepatic impairment (Child-Pugh C). Concomitant use with atazanavir containing products, atorvastatin, simvastatin, dabigatran etexilate, ethinyl oestradiol-containing products, strong P-gp and CYP3A inducers, such as rifampicin, carbamazepine, St. John's wort, phenobarbital, phenytoin, and primidone.
Special warnings and precautions for use:
Hepatitis B virus reactivation
Cases of hepatitis B virus (HBV) reactivation, some of them fatal, have been reported during or after treatment with direct-acting antiviral agents. HBV screening should be performed in all patients before initiation of treatment.
Hepatic impairment
MAVIRET is not recommended in patients with moderate hepatic impairment (Child-Pugh B).
Patients who failed a prior regimen containing an NS5A- and/or an NS3/4A-inhibitor
MAVIRET is not recommended for the re-treatment of patients with prior exposure to NS3A/4A and/or NS5A-inhibitors.
Use in diabetic patients
Diabetics may experience improved glucose control and potential symptomatic hypoglycaemia after initiating HCV direct acting antiviral treatment. Glucose levels should be closely monitored, particularly within the first 3 months of treatment.
Adverse Reactions
Most common (≥10%) adverse reactions for MAVIRET were headache and fatigue.
This is not a complete summary of all safety information. See MAVIRET full summary of product characteristics (SmPC) at www.ema.europa.eu. Globally, prescribing information varies; refer to the individual country product label for complete information.
About AbbVie
AbbVie is a global, research and development-based biopharmaceutical company committed to developing innovative advanced therapies for some of the world's most complex and critical conditions. The company's mission is to use its expertise, dedicated people and unique approach to innovation to markedly improve treatments across four primary therapeutic areas: immunology, oncology, virology and neuroscience. In more than 75 countries, AbbVie employees are working every day to advance health solutions for people around the world. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, LinkedIn or Instagram.
Forward-Looking Statements
Some statements in this news release are, or may be considered, forward-looking statements for purposes of the Private Securities Litigation Reform Act of 1995. The words "believe," "expect," "anticipate," "project" and similar expressions, among others, generally identify forward-looking statements. AbbVie cautions that these forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially from those indicated in the forward-looking statements. Such risks and uncertainties include, but are not limited to, competition from other products, challenges to intellectual property, difficulties inherent in the research and development process, adverse litigation or government action, and changes to laws and regulations applicable to our industry. Additional information about the economic, competitive, governmental, technological and other factors that may affect AbbVie's operations is set forth in Item 1A, "Risk Factors," of AbbVie's 2018 Annual Report on Form 10-K, which has been filed with the Securities and Exchange Commission. AbbVie undertakes no obligation to release publicly any revisions to forward-looking statements as a result of subsequent events or developments, except as required by law.
___________________________
*Patients who achieve a sustained virologic response at 12 weeks post treatment (SVR12) are considered cured of hepatitis C.
**The recommended duration of MAVIRET is 12 weeks in liver or kidney transplant recipients with or without cirrhosis.
1 Brown RS, Hezode C, Wang S, et al. Preliminary Efficacy and Safety of 8-Week Glecaprevir/Pibrentasvir in Patients with HCV Genotype 1–6 Infection and Compensated Cirrhosis: The EXPEDITION-8 Study. Presented at The Liver Meeting®, the Annual Meeting of the American Association for the Study of Liver Diseases (AASLD) in San Francisco, U.S., November 13, 2018
2 MAVIRET™ tablets (glecaprevir/pibrentasvir) Summary of product characteristics. Ludwigshafen, Germany: AbbVie Deutschland GmbH & Co. KG.
Copyright 2019 PR Newswire
Also a large buy by a director:
https://twitter.com/DewDiligence/status/1157031064931581952
EVP, Chief Strategy Officer of Abbvie Inc (30-Year Financial, Insider Trades) Henry O Gosebruch (insider trades) bought 30,000 shares of ABBV on 07/29/2019 at an average price of $67.28 a share. The total cost of this purchase was $2 million.
https://finance.yahoo.com/news/abbvie-inc-abbv-evp-chief-221505814.html
Was hoping it would go back into the 60's. I was willing to buy it in the low 70's so I picked up more today.
cooler
$ABBV AbbVie (ABBV) Tops Q2 EPS by 6c, Revenue Beats, Updates FY Guidance
https://www.streetinsider.com/Earnings/AbbVie+%28ABBV%29+Tops+Q2+EPS+by+6c%2C+Revenue+Beats%2C+Updates+FY+Guidance/15740794.html
$ABBV watch for the short squeeze this Friday
Nice. Thank you! I’ll be driving past ABVIE today.
Received. Thank you.
Way oversold and should be bounce back this week
I’m in. We live near their North Suburbs facilities outside Chicago. Very impressive grounds. Thanks for the research I read on the board here.
$ABBV AbbVie (ABBV) Upgraded to Buy: Here's What You Should Know ABBV
https://finance.yahoo.com/news/abbvie-abbv-upgraded-buy-heres-130001195.html
Reload the dip yesterday for the dividend
Thanks Sir and you are the best trader as well
you called it
you earn the props
Ugotta give credit
to where credit is due
imo
Haha...thanks for that
good call mighty warrior, AGN as well
https://investorshub.advfn.com/boards/read_msg.aspx?message_id=149587951&txt2find=ABBV
keep the solid picks coming
we appreciate them
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