Stock SCLX SCILEX HOLDING COMPANY
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SCLX

US80880W1062

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 04:00:00 2024-05-07 pm EDT 		5-day change 1st Jan Change
0.9173 USD +5.98% Intraday chart for Scilex Holding Company +7.51% -55.03%
Apr. 16 Scilex Issues Preliminary Q1 Sales Results for ZTlido MT
Mar. 20 Scilex Seeks FDA Approval to Add Dosing Guidance to Gout Treatment Drug Label MT

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Scilex Holding Company Announces $15 Million Registered Direct Offering
AQ
Scilex Holding Company Provides Certain Preliminary Unaudited Financial Results for Gross and Net Sales for ZTlido for the First Quarter 2024
AQ
Scilex Issues Preliminary Q1 Sales Results for ZTlido
MT
Scilex Holding Company Provides Certain Preliminary Unaudited Financial Results For Gross and Net Sales for ZTlido® for the First Quarter 2024; Implements Planned 2024 Commercial Ramp for Additional Opioid Sparing Product and Reduction of R&D and Other Administrative Expenses
AQ
Scilex Holding Company Announces Launching of Co-Pay Programs for Both ZTlido and ELYXYB for Commercially Insured Patients and the addition of ELYXYB to a Multi-State Medicaid Pharmaceutical Purchasing Group
AQ
Scilex Holding Company Announces Launching of Co-Pay Programs for Both ZTlido® and ELYXYB® for Commercially Insured Patients and the addition of ELYXYB® to a Multi-State Medicaid Pharmaceutical Purchasing Group to Its Purchasing Pool
AQ
Scilex : Submission of Matters to a Vote of Security Holders - Form 8-K
PU
Scilex Holding Company Announces that the U.S. Bankruptcy Court has Extended the Lockup Period on Shares of Scilex Stock Previously Distributed by Sorrento to its Stockholders as a Dividend
AQ
Scilex Holding Company Announces New Out-of-Pocket Costs for Commercially Insured Patients
AQ
Scilex Seeks FDA Approval to Add Dosing Guidance to Gout Treatment Drug Label
MT
Scilex Settles Patent Dispute With Takeda Pharmaceutical Over Gloperba
MT
Scilex Holding Company Announces Seeking Approval from the FDA for Modification of the Gloperba® Label to Provide Specific Dosing Guidance for Patients with Renal Impairment and Other Circumstances Where Dose Adjustment is Needed
AQ
Scilex Holding Company Announces Seeking Approval from the FDA for Modification of the Gloperba®? Label to Provide Specific Dosing Guidance for Patients with Renal Impairment and Other Circumstances Where Dose Adjustment Is Needed
CI
Scilex Holding Company Announces a Settlement Agreement with Takeda Pharmaceuticals to Resolve the Paragraph IV Patent Infringement Lawsuit Relating to Scilex’s Filing of a sNDA with the FDA Seeking to Expand the Label for its FDA-Approved Liquid Colchicine Product, Gloperba®
AQ
Scilex Holding Company Announces Repayment in Full of the Remaining Balance of Convertible Debentures and Early Payment of the Senior Secured Promissory Note, Paving the Way for Future Growth and Innovation
AQ
Scilex Holding Company Provides Responses to Product Composition Questions Related to its ELYXYB® Patent in Canada for a New Drug Submission Under Review by Health Canada for the Approval of ELYXYB® for Acute Treatment of Migraine With or Without Aura in Canada
AQ
Scilex Holding Company Provides Responses to Product Composition Questions Related to Its ELYXYB® Patent in Canada
CI
Scilex Holding Announces Issuance of Halal Certification for its ZTlido® product by Circle H International, Inc.
AQ
Scilex Settles Claims in Case Against Virpax for $6 Million, 6% Royalties From Three Drugs
MT
Scilex Holding Company’s Wholly Owned Subsidiary, Scilex Pharmaceuticals Inc., Entered into a Definitive Mutual Release and Settlement Agreement with Virpax Pharmaceuticals, Inc. Relating to the Previously Announced Term Sheet with Virpax in Respect of Such Release and Settlement
AQ
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