$PEPG

PepGen Inc.

PepGen is a clinical-stage biotechnology company developing oligonucleotide therapeutics for severe neuromuscular and neurologic diseases. Its Enhanced Delivery Oligonucleotide platform uses cell-penetrating peptides conjugated to oligonucleotide cargo to promote cellular uptake and delivery to the nucleus. PepGen’s lead product candidate, PGN-EDODM1, is being developed for myotonic dystrophy type 1. It is designed to bind expanded repeats in DMPK messenger RNA and release the RNA-binding protein MBNL1, with the aim of correcting disease-related RNA splicing. The candidate uses a peptide-conjugated morpholino oligonucleotide. PepGen’s clinical development program for PGN-EDODM1 includes the completed Phase 1 FREEDOM study, the Phase 2 FREEDOM2 study and the FREEDOM-OLE open-label extension study. The company also develops its EDO platform for potential use with other oligonucleotide cargos. PepGen is headquartered in Boston, Massachusetts.

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PepGen GAAP EPS of -$0.28 misses by $0.01 (NASDAQ:PEPG)

PepGen (PEPG) reported a Q3 GAAP EPS of -$0.28, missing estimates by $0.01. The company had $104.8M in cash and equivalents as of September 30, 2026, and expects this to fund operations into 2028.

PepGen Reports Third Quarter 2026 Financial Results

PepGen Inc. (PEPG) filed an SEC Form 8-K — Results of Operations and Financial Condition. PepGen Reports Third Quarter 2026 Financial Results and Recent Corporate Highlights – Positive FREEDOM2-DM1 10 mg/kg cohort results demonstrated highest reported splicing correction and improvements across multiple functional measures – – 12.5 mg/kg FREEDOM2-DM1 cohort fully enro

PEPG sentiment & insider activity

Over the past 7 days, AlphAI's AI scored 10 news stories mentioning PEPG (PepGen Inc.). Coverage has skewed bullish: 8 bullish, 0 neutral, and 2 bearish.

Recent PEPG coverage spans earnings, financial news and market movers.

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PepGen Reports Third Quarter 2026 Financial Results

PepGen Inc. (PEPG) filed an SEC Form 8-K — Results of Operations and Financial Condition. PepGen Reports Third Quarter 2026 Financial Results and Recent Corporate Highlights – Positive FREEDOM2-DM1 10 mg/kg cohort results demonstrated highest reported splicing correction and improvements across multiple functional measures – – 12.5 mg/kg FREEDOM2-DM1 cohort fully enro

PepGen 3Q 2026: EPS ($0.28) — 10-Q Summary

PepGen reported no revenue and a net loss of $19.39M for 3Q 2026, with higher R&D and clinical trial costs. EPS improved to ($0.28) from ($0.52) YoY. FREEDOM2 trial showed 46.5% splicing correction at 10 mg/kg, but remains on partial clinical hold. PepGen enrolled 19 participants in FREEDOM-OLE and discontinued DMD-related R&D.

PepGen Inc. (PEPG): Submission of Matters to a Vote of Security Holders

PepGen Inc. (PEPG) filed an SEC Form 8-K — Submission of Matters to a Vote of Security Holders. 8-K false 0001835597 0001835597 2026-06-18 2026-06-18 UNITED STATES SECURITIES AND EXCHANGE COMMISSION WASHINGTON, D.C. 20549 FORM 8-K CURRENT REPORT Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 Date of Report (Date of earliest event reported): June 18,

Buy Rating on PepGen: DM1 Program De-Risked by Stronger Underlying Biology and Upside from Higher-Dose Cohorts

H.C. Wainwright analyst Ananda Ghosh maintained a Buy rating on PepGen Inc. with a $20.00 price target. Ghosh believes PepGen's DM1 program is de-risked due to stronger underlying biology observed in treated patients, despite a modest average splicing correction skewed by an anomalous patient. The analyst anticipates significant upside from higher-dose cohorts, expecting materially higher splicing correction which could serve as a key value inflection point for the stock.

PepGen stock tumbles 44% on disappointing trial results

PepGen Ltd (NASDAQ:PEPG) shares dropped 44% after-hours following disappointing Phase 2 trial results for its myotonic dystrophy type 1 treatment, PGN-EDODM1. The drug showed an average splicing correction of 7.3% compared to placebo, with an outlier patient significantly impacting the overall mean. Despite the setback, the company plans to report data from a higher dose cohort in late 2026 and has sufficient funding into mid-2027.

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