Endo International plc (ENDP)
(Delayed Data from NSDQ)
$8.20 USD
+0.48 (6.22%)
Updated May 3, 2019 04:00 PM ET
After-Market: $8.19 (%) 5:22 PM ET
NA Value
NA Growth NA Momentum NA VGMWe use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies, revised Privacy Policy and Terms of Service.
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$8.20 USD
+0.48 (6.22%)
Updated May 3, 2019 04:00 PM ET
After-Market: $8.19 (%) 5:22 PM ET
NA Value
NA Growth NA Momentum NA VGM
Zacks News
Endo International (ENDP) Gains But Lags Market: What You Should Know
by Zacks Equity Research
Endo International (ENDP) closed at $3.21 in the latest trading session, marking a +0.63% move from the prior day.
Is Endo International (ENDP) a Great Stock for Value Investors?
by Zacks Equity Research
Is Endo International (ENDP) a great pick from the value investor's perspective right now? Read on to know more.
Endo International (ENDP) Outpaces Stock Market Gains: What You Should Know
by Zacks Equity Research
Endo International (ENDP) closed the most recent trading day at $3.22, moving +0.31% from the previous trading session.
Endo International (ENDP) Stock Moves -0.9%: What You Should Know
by Zacks Equity Research
Endo International (ENDP) closed at $3.32 in the latest trading session, marking a -0.9% move from the prior day.
Endo International (ENDP) Stock Sinks As Market Gains: What You Should Know
by Zacks Equity Research
Endo International (ENDP) closed at $3.27 in the latest trading session, marking a -1.8% move from the prior day.
Endo International (ENDP) Dips More Than Broader Markets: What You Should Know
by Zacks Equity Research
In the latest trading session, Endo International (ENDP) closed at $3.55, marking a -1.11% move from the previous day.
JAZZ's Xywav Gets Orphan Drug Exclusivity for Hypersomnia
by Zacks Equity Research
The FDA bestows an Orphan Drug Exclusivity to Jazz's (JAZZ) Xywav for treating idiopathic hypersomnia in adults. This is the second Orphan Drug Exclusivity for the drug.
Jazz (JAZZ) Enrolls First Patient in Psychiatric Disorder Study
by Zacks Equity Research
Jazz Pharmaceuticals (JAZZ) enrolls the first patient in a phase II study to evaluate JZP150 for treating adults with post-traumatic stress disorder.
Can-Fite (CANF) Files Patent Applications for Namodenoson
by Zacks Equity Research
Can-Fite (CANF) files patent applications in several countries for treating all advanced solid tumors. The filing comes after Can-Fite's drug cleared all tumor lesions in advanced liver cancer.
AstraZeneca (AZN) Closes Agreement for Eplontersen With Ionis
by Zacks Equity Research
AstraZeneca (AZN) closes its agreement with Ionis for jointly developing and commercializing eplontersen in the United States.
Pluristem (PSTI) Misses Study Goal to Treat COVID-Related ARDS
by Zacks Equity Research
Pluristem's (PSTI) phase II studies evaluating PLX-PAD cells for treating acute respiratory distress syndrome associated with COVID-19 fail to achieve the primary endpoint.
ChemoCentryx's (CCXI) Stock Increases on Tavneos' FDA Nod
by Zacks Equity Research
ChemoCentryx's (CCXI) Tavneos gives a significant boost to the company, following its FDA approval in ANCA-associated vasculitis. The drug is also being evaluated in other indications.
Novartis (NVS) Gets FDA Nod for Cosentyx's Label Expansion
by Zacks Equity Research
The FDA approves Novartis' (NVS) Cosentyx for the treatment of children and adolescents with enthesitis-related arthritis and psoriatic arthritis.
AstraZeneca's (AZN) Ultomiris sBLA Gets FDA Priority Review
by Zacks Equity Research
The FDA accepts and grants priority review to AstraZeneca's (AZN) sBLA for Ultomiris for treating adults with generalized myasthenia gravis. A decision is expected in the second quarter of 2022.
Jazz (JAZZ) Enrols First Patient in Essential Tremor Study
by Zacks Equity Research
Jazz Pharmaceuticals (JAZZ) enrolls the first patient in a phase IIb study to evaluate JZP385 for essential tremor.
AbbVie (ABBV) Rinvoq Gets FDA Nod for Active Psoriatic Arthritis
by Zacks Equity Research
The FDA approves AbbVie's (ABBV) Rinvoq for the treatment of adults with active psoriatic arthritis. This is the second FDA-approved indication for the drug.
Intellia (NTLA) Begins Dosing in Hereditary Angioedema Study
by Zacks Equity Research
Intellia (NTLA) doses the first patient in a phase I/II study to evaluate NTLA-2002 as a single-dose therapy for preventing attacks in patients having hereditary angioedema.
Angion (ANGN) Kidney Drug Misses Third Study Goal in 2021
by Zacks Equity Research
Angion's (ANGN) phase II study evaluating ANG-3777 in cardiac surgery-associated acute kidney injury fails to achieve the primary endpoint.
Lilly (LLY) Inks Metabolic Disorders Therapy Development Deal
by Zacks Equity Research
Lilly (LLY) inks a strategic collaboration with Regor Therapeutics to discover and develop novel therapies for metabolic disorders.
Heron's (HRTX) Zynrelef Gets FDA Nod for Label Expansion
by Zacks Equity Research
The FDA grants label expansion to Heron???s (HRTX) Zynrelef for pain relief after small to medium abdominal surgeries, lower extremity total joint replacements, and foot and ankle surgeries in adults.
Recursion (RXRX) Inks Neuroscience and Oncology Deal With Roche
by Zacks Equity Research
Recursion (RXRX) inks a collaboration with Roche to identify novel targets and advance medicines in areas of neuroscience and oncology indication. Shares rise.
Sanofi's (SNY) Filing for Rare Disease Drug Accepted by EMA
by Zacks Equity Research
The EMA accepts Sanofi's (SNY) regulatory submission seeking approval for olipudase alfa, a potential treatment for acid sphingomyelinase deficiency.
Merck (MRK) Pauses Enrolment in HIV-1 Prevention Studies
by Zacks Equity Research
Merck (MRK) pauses enrolment for two phase III studies evaluating islatravir for pre-exposure prophylaxis of HIV-1 infection, following the recommendation of an external data monitoring committee.
Bayer's (BAYRY) Phase III Study on Nubeqa Combo Meets Goal
by Zacks Equity Research
Bayer's (BAYRY) phase III study evaluating Nubeqa in combination with docetaxel and androgen deprivation therapy for treating metastatic hormone-sensitive prostate cancer meets the primary endpoint.
Amicus (FOLD) Filings for AT-GAA in Pompe Disease Accepted by EMA
by Zacks Equity Research
The European Medicines Agency accepts Amicus Therapeutics' (FOLD) MAA for AT-GAA, a potential treatment for Pompe disease.