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SCLX

US80880W1062

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04-16	Scilex Issues Preliminary Q1 Sales Results for ZTlido	MT
03-20	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	04-24	AQ
Scilex Holding Company Provides Certain Preliminary Unaudited Financial Results for Gross and Net Sales for ZTlido for the First Quarter 2024	04-17	AQ
Scilex Issues Preliminary Q1 Sales Results for ZTlido	04-16	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	04-16	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	04-10	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	04-09	AQ
Scilex : Submission of Matters to a Vote of Security Holders - Form 8-K	04-05	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	03-27	AQ
Scilex Holding Company Announces New Out-of-Pocket Costs for Commercially Insured Patients	03-21	AQ
Scilex Seeks FDA Approval to Add Dosing Guidance to Gout Treatment Drug Label	03-20	MT
Scilex Settles Patent Dispute With Takeda Pharmaceutical Over Gloperba	03-20	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	03-20	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	03-20	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®	03-20	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	03-19	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	03-18	AQ
Scilex Holding Company Provides Responses to Product Composition Questions Related to Its ELYXYB® Patent in Canada	03-18	CI
Scilex Holding Announces Issuance of Halal Certification for its ZTlido® product by Circle H International, Inc.	03-15	AQ
Scilex Settles Claims in Case Against Virpax for $6 Million, 6% Royalties From Three Drugs	03-15	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	03-15	AQ

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