Financials
Cash Data
- Monthly Burn
- Burn Trend
- Dilution Risk
- SEC Filing
Key Stats
Upcoming Catalysts
FDA decisions, readouts and PDUFA dates · scored by probability of approval
PEPG Catalyst Timeline
Dated clinical, regulatory and corporate events for PepGen Inc.
Catalyst Timeline
Dated clinical, regulatory & corporate events for PepGen Inc.
Upcoming catalysts 2
Event history 50
Past FDA Catalysts and PDUFA Decisions
How PEPG actually traded into and out of each decision
| Date | Drug | Catalyst | Stage | Reaction | Event Move % | Best Trade % |
|---|---|---|---|---|---|---|
| 2025-09-30 | PGN-EDO51 | Phase 2 data readout | Phase 2 |
Drug Pipeline Intelligence
| Drug | Indication | Phase | PTRS | rNPV | Status | Enroll | Velocity | Design | Est. Completion | ML Signal | Last Change |
|---|---|---|---|---|---|---|---|---|---|---|---|
| PGN-EDODM1 Small moleculeNCT06667453 | Myotonic Dystrophy 1 | Phase 2 | RECRUITING | 72 | Mar 1, 2027 |
Clinical Trial Results
Readouts, endpoints and source filings for every PEPG program
| Drug Name | Indication | Phase | Date | Trial Results Summary | Title | Source |
|---|---|---|---|---|---|---|
| PGN-EDODM1 Fast TrackOrphan | Myotonic Dystrophy Type 1 (DM1) | Phase 1 | 2026-03-05 | splicing correction: 5 mg/kg 12.3%, 10 mg/kg 29.1%, 15 mg/kg 53.7%; safety: PGN-EDODM1 was generally well-tolerated across all doses; treatment-emergent adverse events (TEAEs) were mild to moderate, transient, and required no intervention.Read More | PepGen Reports Fourth Quarter and Year-End 2025 Financial Results and Recent Corporate HighlightsRead More |
Inside Trades
| Insider | Side | Shares | Price | Value | Date |
|---|---|---|---|---|---|
| Kasraian KasraOfficer (Chief Technical Officer) | Sell | -1,233 50,074 held | $1.41 | 05/21/2026 |
Hedge Fund 13F Activity
Hedge Funds invested in PEPG
| Fund | % of Portfolio | Current MV | Shares Owned | Activity |
|---|---|---|---|---|
| RA CAPITAL MANAGEMENT, L.P. | 0.3 % (-25 %) | 36.12 M | 20.06 M |
PEPG Institutional Ownership Trends
Options Data
Option Volume
Option Chain Statistics
| Expiry | Call Vol | Put Vol | Vol P/C | Call OI | Put OI | OI P/C | IV Call | IV Call OI-Wtd | IV Call Vol-Wtd | IV Put | IV Put OI-Wtd | IV Put Vol-Wtd |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2026-10-16 | ||||||||||||
Real-Time Option Chain
| Calls | Strike | Puts | ||||
|---|---|---|---|---|---|---|
| Last | Vol | OI | Last | Vol | OI | |
| No data available | ||||||
Calls vs Puts by Expiry
Competitive positioning
How PEPG ranks across every disease it competes in
PEPG News
PepGen Reports Second Quarter 2026 Financial Results and Recent Corporate Highlights
PepGen has released its financial results for the second quarter of 2026, alongside recent corporate highlights. The report provides insights into the company's performance and strategic developments during this period. Further details on financial metrics and corporate activities were not disclosed in the provided text.
Read more →PepGen to Advance PGN-EDODM1 Into Highest Dose Cohort in Phase 2 FREEDOM2-DM1 Study Following DSMB Review
PepGen has announced the advancement of its drug PGN-EDODM1 into the highest dose cohort of the Phase 2 FREEDOM2-DM1 study. This decision follows a favorable review by the Data Safety Monitoring Board (DSMB), indicating confidence in the drug's safety and potential efficacy.
Read more →PepGen Announces Presentations at the 15th International Myotonic Dystrophy Consortium Highlighting Clinical Data from the PGN-EDODM1 Program
PepGen has announced its participation in the 15th International Myotonic Dystrophy Consortium. The company will present clinical data related to its PGN-EDODM1 program. Further details regarding the findings or implications of the data were not provided in the announcement.
Read more →Company Presentation May 2026 Forward-Looking Statements This presentation contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. These statements may
PepGen presented forward-looking statements regarding their investigational therapy, PGN-EDODM1, highlighting its potential in treating Myotonic Dystrophy Type 1 (DM1). The presentation stressed the advantages of the EDO platform in facilitating oligonucleotide delivery to nuclei. Positive results from clinical trials indicate an emerging safety profile, while ongoing regulatory discussions play a critical role in the therapy's future. However, potential risks include slow enrollment in clinical trials and the impact of regulatory decisions on development timelines.
Read more →PepGen Reports First Quarter 2026 Financial Results and Recent Corporate Highlights
PepGen has reported its financial results for the first quarter of 2026, along with recent corporate highlights. The details of the financial performance and any significant developments were not disclosed in the article. Further information may be available in subsequent releases.
Read more →PepGen Announces Topline Results from Lowest Dose (5 mg/kg) MAD Cohort in the Ongoing Phase 2 FREEDOM2 Study Demonstrating Favorable Safety, Splicing and vHOT Data
PepGen has announced topline results from the lowest dose cohort in the ongoing Phase 2 FREEDOM2 study. The results indicate favorable safety and splicing data, though specific details are not provided in the article. The study continues to progress as part of PepGen's clinical research efforts.
Read more →PepGen Reports Fourth Quarter and Year-End 2025 Financial Results and Recent Corporate Highlights
PepGen Inc. reported its financial results for Q4 and year-end 2025, highlighting the progress of its PGN-EDODM1 candidate for DM1. The company is well-funded, with sufficient cash to support operations into 2027. Promising data from the FREEDOM trial suggest PGN-EDODM1 could be a leading treatment option, with further results expected from ongoing trials in 2026.
Read more →PepGen Announces Regulatory Updates on FREEDOM2
PepGen Inc. has announced regulatory updates regarding its FREEDOM2 trial, which is currently on partial clinical hold by the FDA due to concerns about preclinical studies. Despite this, the company has received clearance to initiate the trial in South Korea, Australia, and New Zealand, while dosing continues in Canada and the UK. PepGen anticipates reporting data from the trial's cohorts in 2026.
Read more →March 2026 Company Presentation Forward-Looking Statements This presentation contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. These statements ma
PepGen has made advancements with its investigational therapy PGN-EDODM1 for Myotonic Dystrophy Type 1. The company presents forward-looking statements highlighting its therapeutic potential and favorable safety profile of PGN-EDODM1. Regulatory clearances in various countries support ongoing patient enrollment, but the company warns of potential delays and uncertainties in clinical trials and regulatory interactions. The presentation emphasizes the innovative EDO platform’s ability to enhance oligonucleotide therapies.
Read more →PepGen to Participate in the Leerink Global Healthcare Conference
PepGen Inc. will participate in the Leerink Global Healthcare Conference on March 10, 2026. CEO James McArthur will engage in a fireside chat, discussing the company's advancements in oligonucleotide therapies aimed at treating severe neuromuscular and neurological diseases. A webcast of the event will be available for investors.
Read more →PepGen Reports Inducement Grant under Nasdaq Listing Rule 5635(c)(4) to Newly Appointed Chief Business and Legal Officer
PepGen Inc. has awarded a significant inducement grant to its newly appointed Chief Business and Legal Officer, Joseph Vittiglio. The grant includes a non-qualified stock option for 160,000 shares at an exercise price of $5.59, with a vesting schedule over four years. This award is part of PepGen's 2024 Inducement Plan and was approved by the Board of Directors.
Read more →Julia Deutsch Lyra Strategic Advisory Jdeutsch@lyraadvisory.com
PepGen Inc. has appointed Joseph Vittiglio as Chief Business and Legal Officer, drawing from his two decades of experience in the biotechnology sector. Vittiglio's previous roles include positions at bluebird bio and Finch Therapeutics, where he led legal and business development efforts. His appointment comes as PepGen prepares for readouts from its PGN-EDODM1 program in 2026, indicating a strategic move to bolster its executive team during critical phases of development. The company focuses on advancing oligonucleotide therapies for severe neuromuscular and neurological diseases.
Read more →PepGen Reports Third Quarter 2025 Financial Results and Recent Corporate Highlights
PepGen reported strong Q3 2025 financial results, highlighting the successful outcomes from the 15 mg/kg cohort of its FREEDOM study which showed record splicing correction in DM1 patients. The company has enrolled all patients in the 5 mg/kg cohort of the FREEDOM2 study, aimed at further validating their treatment candidate PGN-EDODM1. Additionally, a recent financing round raised $115 million, securing operations through at least mid-2027. The firm plans to share data from the ongoing trials in early 2026, maintaining a focus on improving outcomes for DM1 patients.
Read more →October 2025 Company Presentation Forward-Looking Statements This presentation contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. These statements
PepGen's October 2025 company presentation highlights forward-looking statements regarding its investigational therapy PGN-EDODM1 for Myotonic Dystrophy Type 1. The company emphasizes the potential of its EDO platform in delivering oligonucleotides and the therapy's favorable safety profile, among other milestones. Challenges include risks associated with clinical trial progress and regulatory approvals, which could impact development timelines. The company is positioned well with designations for expedited review in the U.S. and EU.
Read more →PepGen Announces Highest Mean Splicing Correction Reported in DM1 Patients
PepGen announced significant positive results from its clinical trial for PGN-EDODM1, a treatment for myotonic dystrophy type 1 (DM1). In the Phase 1 FREEDOM-DM1 study, a mean splicing correction of 53.7% was observed after a single 15 mg/kg dose, surpassing previous reports. All patients showed improvements in splicing, and the treatment was generally well-tolerated. The company is set to report additional data from its FREEDOM2 trial in early 2026.
Read more →PepGen Announces Proposed Public Offering
PepGen Inc. has announced a proposed public offering of its common stock and pre-funded warrants, aimed at raising funds for its ongoing research and clinical development efforts. This offering is being managed by Leerink Partners and Stifel, who will also have a 30-day option to purchase additional shares. The actual size and conditions of the offering remain uncertain and dependent on market factors. PepGen's EDO platform continues to innovate in the treatment of neuromuscular and neurological diseases.
Read more →PepGen Reports Second Quarter 2025 Financial Results and Recent Corporate Highlights
PepGen Inc. has reported its second-quarter financial results for 2025, highlighting progress in its lead program PGN-EDODM1 for the treatment of myotonic dystrophy type 1. The company has completed dosing in the 15 mg/kg cohort of the FREEDOM trial and is set to report topline results in early Q4 2025. Additionally, they are transitioning to the Phase 2 FREEDOM2 trial, which aims to further investigate the efficacy of multiple ascending doses of the drug. Despite a significant net loss reported this quarter, PepGen expresses confidence in its cash resources extending into mid-2026, supporting its ongoing development efforts.
Read more →PepGen to Focus on Development of Promising DM1 Program Following 10 mg/kg PGN-EDO51 Update
PepGen Inc. announced it will discontinue development of its PGN-EDO51 program for Duchenne muscular dystrophy (DMD) after it failed to meet target dystrophin levels in the CONNECT1-EDO51 trial. The company will shift its focus to its myotonic dystrophy type 1 (DM1) program, which is in Phase 2 clinical trials. The PGN-EDO51 program did show a favorable safety profile, as all treatment-related adverse events were mild. PepGen continues to pursue its DM1 program, expecting significant results from its ongoing trials.
Read more →PepGen Reports First Quarter 2025 Financial Results and Recent Corporate Highlights
PepGen Inc. reported its financial results for Q1 2025, revealing promising initial data for its DM1 treatment PGN-EDODM1 showing a mean splicing correction of 29.1%. The company has upcoming data expected from both the FREEDOM-DM1 and CONNECT1-EDO51 studies in the second half of 2025 and early 2026. Additionally, PepGen is focusing on extending its cash runway and has strengthened its leadership with new Board members. Despite a rising net loss compared to the previous year, the company remains optimistic about its clinical programs.
Read more →PepGen Announces Appointment of Two New Directors to its Board
PepGen Inc. has announced the appointment of two new directors, Lisa Wyman and Dr. Mitchell H. Finer, to its Board of Directors. Both bring extensive experience in the life sciences sector, with proven track records in clinical operations and scientific innovation. Their appointments are seen as a vital addition to the company's leadership as it advances mid-stage clinical trials and aims to leverage its Enhanced Delivery Oligonucleotide platform. PepGen focuses on developing novel therapies for severe neuromuscular and neurological diseases.
Read more →