News PepGen Inc.

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PEPG

US7133171055

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May. 15	PepGen Q1 Loss Narrows	MT
May. 14	PepGen Inc. Reports Earnings Results for the First Quarter Ended March 31, 2024	CI

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PepGen Q1 Loss Narrows	May. 15	MT
PepGen Inc. Reports Earnings Results for the First Quarter Ended March 31, 2024	May. 14	CI
PepGen Reports First Quarter 2024 Financial Results and Recent Corporate Highlights	May. 14	GL
PepGen : Corporate Deck – May 2024	May. 07	PU
PepGen to Participate in Upcoming Investor Conferences	Mar. 13	GL
PepGen to Participate in Upcoming Investor Conferences	Mar. 13	AQ
PepGen Says Potential Duchenne Muscular Dystrophy Treatment Gets FDA Orphan Drug, Rare Pediatric Disease Designations	Mar. 13	MT
PepGen's Rare Muscle Disorder Therapy Gets FDA Orphan Drug, Rare Pediatric Disease Designations	Mar. 13	DJ
PepGen Receives U.S. FDA Orphan Drug and Rare Pediatric Disease Designations for PGN-EDO51 for the Treatment of Duchenne Muscular Dystrophy	Mar. 13	GL
PepGen Receives U.S. FDA Orphan Drug and Rare Pediatric Disease Designations for PGN-EDO51 for the Treatment of Duchenne Muscular Dystrophy	Mar. 13	AQ
Wedbush Trims PepGen's PT to $20 From $21, Incorporates Offering, Adjusts Share Count Assumptions; Maintains Outperform Rating	Mar. 07	MT
Transcript : PepGen Inc., Q4 2023 Earnings Call, Mar 06, 2024	Mar. 06
PepGen Inc. Reports Earnings Results for the Full Year Ended December 31, 2023	Mar. 06	CI
PepGen Reports Fourth Quarter and Full Year 2023 Financial Results and Recent Corporate Developments	Mar. 06	GL
PepGen Reports Fourth Quarter and Full Year 2023 Financial Results and Recent Corporate Developments	Mar. 06	AQ
PepGen Inc. Reports Earnings Results for the Fourth Quarter Ended December 31, 2023	Mar. 06	CI
PepGen Announces Clearance of CTA by UK Medicines & Healthcare Products Regulatory Agency to Begin CONNECT2-EDO51, a Phase 2 Clinical Trial designed to support potential accelerated approval of PGN-EDO51 for the Treatment of Duchenne Muscular Dystrophy	Mar. 04	GL
PepGen Announces Clearance of CTA by UK Medicines & Healthcare Products Regulatory Agency to Begin CONNECT2-EDO51, a Phase 2 Clinical Trial designed to support potential accelerated approval of PGN-EDO51 for the Treatment of Duchenne Muscular Dystrophy	Mar. 04	AQ
PepGen Inc. Announces Clearance of CTA by UK Medicines & Healthcare Products Regulatory Agency to Begin CONNECT2-EDO51, a Phase 2 Clinical Trial designed to support potential accelerated approval of PGN-EDO51 for the Treatment of Duchenne Muscular Dystrophy	Mar. 04	CI
PepGen Says FDA Grants Fast Track Designation to Potential Myotonic Dystrophy Type 1 Treatment	Feb. 20	MT

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