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GABA-A Agent SAGE-217: A New Antidepressant? - Gateway Psychiatric
GABA-A Agent SAGE-217: A New Antidepressant? - Gateway Psychiatric

sage-10k_20181231.htm
sage-10k_20181231.htm

Emboldened By Sage's Zulresso Slip, Marinus Is Set To Succeed In PPD And  Orphan Epilepsy (NASDAQ:MRNS) | Seeking Alpha
Emboldened By Sage's Zulresso Slip, Marinus Is Set To Succeed In PPD And Orphan Epilepsy (NASDAQ:MRNS) | Seeking Alpha

Sage Therapeutics' SAGE-217 Receives FDA's Breakthrough Designation for CNS  Disorders
Sage Therapeutics' SAGE-217 Receives FDA's Breakthrough Designation for CNS Disorders

Sage Therapeutics Announces Development Plan for Zuranolone (SAGE-217)  Following Breakthrough Therapy Guidance Meeting with the U.S. Food & Drug  Administration | Sage Therapeutics, Inc.
Sage Therapeutics Announces Development Plan for Zuranolone (SAGE-217) Following Breakthrough Therapy Guidance Meeting with the U.S. Food & Drug Administration | Sage Therapeutics, Inc.

Sage Therapeutics' Deal With Biogen Should Revive It (NASDAQ:SAGE) |  Seeking Alpha
Sage Therapeutics' Deal With Biogen Should Revive It (NASDAQ:SAGE) | Seeking Alpha

Bait and Switch: the Great Ketamine “Breakthrough” | RxISK
Bait and Switch: the Great Ketamine “Breakthrough” | RxISK

Sage Therapeutics Announces Development Plan for Zuranolone (SAGE-217)  Following Breakthrough Therapy Guidance Meeting with the U.S. Food & Drug  Administration-CliniExpert
Sage Therapeutics Announces Development Plan for Zuranolone (SAGE-217) Following Breakthrough Therapy Guidance Meeting with the U.S. Food & Drug Administration-CliniExpert

Biogen and Sage Therapeutics in Global Collaboration – ISPE Boston
Biogen and Sage Therapeutics in Global Collaboration – ISPE Boston

Sage Therapeutics Phase 3 MOUNTAIN Study of SAGE-217 in Major Depressive  Disorder Does Not Meet
Sage Therapeutics Phase 3 MOUNTAIN Study of SAGE-217 in Major Depressive Disorder Does Not Meet

Sage Therapeutics Receives FDA Breakthrough Therapy Designation for SAGE-217  for the Treatment of Major Depressive Disorder - Chemdiv
Sage Therapeutics Receives FDA Breakthrough Therapy Designation for SAGE-217 for the Treatment of Major Depressive Disorder - Chemdiv

Sage shares up after FDA allows expedited depression drug development
Sage shares up after FDA allows expedited depression drug development

Sage advice: psychiatric drug development is tough | Evaluate
Sage advice: psychiatric drug development is tough | Evaluate

Sage Therapeutics and Biogen Report Positive Phase 3 Data Showing  Zuranolone Significantly Reduced Depressive Symptoms After Two Weeks
Sage Therapeutics and Biogen Report Positive Phase 3 Data Showing Zuranolone Significantly Reduced Depressive Symptoms After Two Weeks

Sage Therapeutics Reports Topline Results from Pivotal Phase 3 MOUNTAIN  Study of SAGE-217 in Major Depressive Disorder
Sage Therapeutics Reports Topline Results from Pivotal Phase 3 MOUNTAIN Study of SAGE-217 in Major Depressive Disorder

Keeping up with the clinical advances: depression | CNS Spectrums |  Cambridge Core
Keeping up with the clinical advances: depression | CNS Spectrums | Cambridge Core

Zuranolone - Wikipedia
Zuranolone - Wikipedia

Sage surges after depression drug gets rapid path to approval - PMLiVE
Sage surges after depression drug gets rapid path to approval - PMLiVE

Sage Therapeutics Forges $575 Million Deal With Shionogi to Market  Depression Drug in Parts of Asia | BioSpace
Sage Therapeutics Forges $575 Million Deal With Shionogi to Market Depression Drug in Parts of Asia | BioSpace

Sage Therapeutics Announces Promising Zuranolone Phase 3 Findings for Major  Depression
Sage Therapeutics Announces Promising Zuranolone Phase 3 Findings for Major Depression

Sage Therapeutics surges 70% after depression drug breakthrough
Sage Therapeutics surges 70% after depression drug breakthrough

Sage Therapeutics and Biogen Announce Positive Pivotal Phase 3 Results for  Zuranolone, an Investigational Two-Week, Once-Daily Therapeutic Being  Evaluated for Major Depressive Disorder | Business Wire
Sage Therapeutics and Biogen Announce Positive Pivotal Phase 3 Results for Zuranolone, an Investigational Two-Week, Once-Daily Therapeutic Being Evaluated for Major Depressive Disorder | Business Wire

SAGE Therapeutics shares rocket after FDA clearance to expedite its  depression post-partum drug SAGE-217
SAGE Therapeutics shares rocket after FDA clearance to expedite its depression post-partum drug SAGE-217

Sage Therapeutics and Biogen Announce New Analyses from the LANDSCAPE  Clinical Development Program of Zuranolone in MDD Presented at the American  College of Neuropsychopharmacology (ACNP) Congress | Business Wire
Sage Therapeutics and Biogen Announce New Analyses from the LANDSCAPE Clinical Development Program of Zuranolone in MDD Presented at the American College of Neuropsychopharmacology (ACNP) Congress | Business Wire

Sage Therapeutics: Zuranolone's Multi-Billion Dollar Market Opportunity  More Than Justifies Company Valuation (NASDAQ:SAGE) | Seeking Alpha
Sage Therapeutics: Zuranolone's Multi-Billion Dollar Market Opportunity More Than Justifies Company Valuation (NASDAQ:SAGE) | Seeking Alpha

sage-10k_20161231.htm
sage-10k_20161231.htm

Here's Why Sage Therapeutics Rose as Much as 20.3% Today | The Motley Fool
Here's Why Sage Therapeutics Rose as Much as 20.3% Today | The Motley Fool

Sage Therapeutics Reports Positive Top-Line Results from Phase II  Placebo-Controlled Trial of SAGE-217 in MDD - Drug Discovery and Development
Sage Therapeutics Reports Positive Top-Line Results from Phase II Placebo-Controlled Trial of SAGE-217 in MDD - Drug Discovery and Development

Sage Therapeutics Reports Topline Results from Pivotal Phase 3 MOUNTAIN  Study of SAGE-217 in Major Depressive Disorder | Business Wire
Sage Therapeutics Reports Topline Results from Pivotal Phase 3 MOUNTAIN Study of SAGE-217 in Major Depressive Disorder | Business Wire