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CA23256X1006

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Cybin Provides Corporate Provides Update Highlighting Recent Clinical Accomplishments and Key Upcoming Catalysts Across Its Development Pipeline	05-06
Sector Update: Health Care Stocks Softer Friday Afternoon	03-15
Cybin Starts Phase 2 Proof-of-Concept Study in Generalized Anxiety Disorder	03-15
Cybin Inc. Initiates Phase 2 Proof-Of-Concept Study of Cyb004 in Generalized Anxiety Disorder	03-15
Cybin berichtet über ein positives Treffen mit der FDA zum Ende der Phase 2 für CYB003 bei schweren depressiven Störungen und über die Planung eines Programms der Phase 3	03-14
Cybin annonce une réunion positive avec la FDA à la fin de la phase 2 pour le CYB003 dans le trouble dépressif majeur et la conception du programme de phase 3	03-14
Cybin Reaches Alignment With FDA on Late-Stage Design For Major Depressive Disorder Trial	03-14
Cybin Inc. Announces Positive End-Of-Phase 2 Meeting with FDA for CYB003 in Major Depressive Disorder and Phase 3 Program Design	03-14
Cybin reçoit la désignation de thérapie innovante de la FDA pour sa molécule psychédélique CYB003 et annonce des données de durabilité positives à quatre mois pour le traitement du trouble dépressif majeur	03-13
Annonce d’un placement privé sursouscrit de 150 millions USD	03-13
Cybin erhält von der FDA den Status eines Therapiedurchbruchs für sein neuartiges psychedelisches Molekül CYB003 und gibt positive Daten zur viermonatigen Dauerhaftigkeit bei schwerer depressiver Störung bekannt	03-13
Sector Update: Health Care Stocks Ease Wednesday Afternoon	03-13
Ankündigung einer überzeichneten Privatplatzierung von 150 Millionen US-Dollar	03-13
Cybin Says Depression Drug Granted Breakthrough Designation by FDA; Raises $150 Million in Private Placement; Shares Jump	03-13
Cybin Inc. Receives FDA Breakthrough Therapy Designation for Its Novel Psychedelic Molecule CYB003 and Announces Positive Four-Month Durability Data in Major Depressive Disorder	03-13
Cybin Inc. Reports Earnings Results for the Third Quarter and Nine Months Ended December 31, 2023	02-14
Cybin Gets FDA Clearance for Generalized Anxiety Disorder Study	01-23
Cybin Announces FDA Clearance to Initiate a Phase 2a Study of CYB004 in Generalized Anxiety Disorder	01-23
Cybin Inc. Announces Positive Topline Data from Phase 1 Studies of Proprietary Deuterated DMT Molecules CYB004 and SPL028	01-08
Cybin Inc. Announces Recent Positive Phase 2 CYB003 Topline Results in MDD and Outlines Key Upcoming Milestones Across its Clinical Development Programs	01-04

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