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enGene Holdings (ENGN)

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Earnings summaries and quarterly performance for enGene Holdings.

Research analysts covering enGene Holdings.

Recent press releases and 8-K filings for ENGN.

enGene Holdings Inc. Amends Loan Agreement and Issues Warrants
ENGN
Debt Issuance
  • enGene Holdings Inc. entered into a Second Amendment to its Amended & Restated Loan and Security Agreement on January 20, 2026, with Lenders and Hercules Capital, Inc..
  • In connection with this amendment, the company issued 40,850 2026 Warrants to Lenders on the Closing Date, with an exercise price of $9.18 per share, exercisable for seven years. The maximum number of 2026 Warrants that can be issued is 204,248, tied to a total commitment of $125,000,000 in 2026 Term Loans.
  • The amended agreement introduces new financial covenants, including maintaining Unrestricted Cash of $10,000,000, which increases to $22,500,000 after a Minimum Cash Trigger Event. A Performance Covenant also requires Net Product Revenue to be at least 65% of the Commercial Revenue Forecast if 2026 Term Loans exceed $60,000,000, with specific waiver conditions.
Jan 21, 2026, 9:05 PM
enGene Announces Expanded Debt Facility with Hercules Capital
ENGN
Debt Issuance
New Projects/Investments
  • enGene Holdings Inc. has entered into an amendment to its loan agreement with Hercules Capital, Inc. for up to US$125 million.
  • This expanded debt facility provides additional financial flexibility to advance detalimogene development and commercialization for bladder cancer, including preparation for a Biologics License Application (BLA) filing in the second half of 2026 and potential commercial launch in 2027.
  • $25 million was funded at the close of the amendment to refinance existing debt, with an additional $75 million available in three tranches upon achieving certain clinical, regulatory, and commercial milestones.
  • A final $25 million tranche may be made upon request of the company and at the discretion of Hercules.
  • The principal amount outstanding and accrued interest under the loan agreement are to be repaid on or before January 1, 2030.
Jan 21, 2026, 12:38 PM
enGene Holdings Inc. Announces Full Year 2025 Financial Results and Business Updates
ENGN
Earnings
Guidance Update
New Projects/Investments
  • enGene Holdings Inc. reported a net loss attributable to common shareholders of $117.3 million, or $2.29 per share, for the full year ended October 31, 2025, with total operating expenses of $123.2 million.
  • As of October 31, 2025, cash, cash equivalents, and marketable securities were $202.3 million, and with an additional $140.1 million in net proceeds from a November public offering, the company expects its cash runway to extend into the second half of 2028.
  • Enrollment for the LEGEND pivotal cohort was completed with 125 patients, and preliminary data showed a 62% complete response rate at 6 months in post-amendment patients.
  • The company plans a Biologic License Application (BLA) submission for detalimogene in the second half of 2026 and has been selected for the FDA's CDRP Program.
Dec 22, 2025, 9:04 PM
enGene Holdings Provides Update on Detalimogene Voraplasmid Development and Financial Runway
ENGN
Product Launch
Guidance Update
New Projects/Investments
  • enGene Holdings is developing detalimogene voraplasmid, a non-viral genetic therapy for non-muscle invasive bladder cancer (NMIBC), a disease with a large market forecast.
  • The company anticipates near-term catalysts including a data update in H2 2026 and a BLA filing and potential launch in 2027.
  • In the registrational LEGEND study, patients treated under the updated protocol showed a six-month complete response rate of 62% and an anytime response rate of 63%.
  • enGene has secured CDRP and RMAT designations from the FDA, which are anticipated to streamline manufacturing and review processes.
  • A recent fundraise has extended the company's cash runway into 2028.
Dec 2, 2025, 5:10 PM
enGene Holdings provides clinical and regulatory updates for detalimogene voraplasmid
ENGN
New Projects/Investments
Guidance Update
  • enGene Holdings' lead product, detalimogene voraplasmid, a non-viral genetic therapy for non-muscle invasive bladder cancer (NMIBC), demonstrated a 62% complete response rate at six months and a 63% anytime response rate in post-protocol patients from the LEGEND study.
  • The company announced it was awarded CDRP designation on December 2, 2025, which is expected to streamline the manufacturing process at review time, complementing its existing RMAT designation.
  • Key upcoming milestones include a data update in the second half of 2026, followed by a BLA filing and potential launch in 2027.
  • A recent fundraise has extended the company's cash runway into 2028.
Dec 2, 2025, 5:10 PM
enGene Holdings Provides Update on Detalimogene Voraplasmid Clinical Development
ENGN
New Projects/Investments
Product Launch
  • enGene Holdings is developing detalimogene voraplasmid, a non-viral gene therapy for non-muscle invasive bladder cancer (NMIBC), which is currently in a registrational study.
  • The LEGEND study for BCG-unresponsive NMIBC patients with carcinoma in situ recently reported a six-month complete response rate of 62% and an anytime response rate of 63% in post-protocol patients, showing a meaningful improvement over pre-protocol results.
  • The company has received CDRP designation for increased correspondence around CMC and RMAT designation for its product.
  • Key upcoming catalysts include a data update in the second half of 2026, a BLA filing, and a potential launch in 2027.
  • Following a recent fundraise, enGene's cash runway has been updated to extend into 2028.
Dec 2, 2025, 5:10 PM
enGene Provides Update on Detalimogene Voraplasmid Development and Market Opportunity
ENGN
New Projects/Investments
Guidance Update
Product Launch
  • enGene is developing detalimogene voraplasmid, a non-viral gene therapy for non-muscle invasive bladder cancer (NMIBC), targeting a market projected to grow to over $20 billion.
  • The product demonstrated a 62% six-month complete response rate in a pivotal program for BCG-unresponsive NMIBC patients, with favorable tolerability (mostly grade 1 or 2 AEs at 42%) and low dose interruptions (1.6%).
  • enGene plans a data update and regulatory filing in the second half of next year (2026), with potential approval in 2027.
  • The company recently raised over $100 million, providing a financial runway into 2027.
Nov 18, 2025, 8:30 AM
enGene Provides Update on Detalimogene Voraplasmid Development and Financial Position
ENGN
Product Launch
New Projects/Investments
Guidance Update
  • enGene is developing detalimogene voraplasmid, a non-viral gene therapy for non-muscle invasive bladder cancer (NMIBC), which is currently in a pivotal program.
  • The company plans a data update and regulatory filing in the second half of 2026, with potential approval in 2027.
  • Recent data from the LEGEND trial showed a six-month complete response rate of 62% for patients in the new protocol cohort, demonstrating competitive efficacy and favorable tolerability with 42% grade 1 or 2 adverse events.
  • enGene recently completed a fundraising round, raising over $100 million, providing capital runway into 2027.
  • The NMIBC market is projected to grow to over $20 billion, and detalimogene is positioned for community urologists due to its ease of use and competitive profile.
Nov 18, 2025, 8:30 AM
enGene Announces Pricing of $130 Million Public Offering
ENGN
  • enGene Holdings Inc. priced a public offering on November 12, 2025, consisting of 12,558,823 common shares at $8.50 per share and 2,735,295 pre-funded warrants at $8.4999 per pre-funded warrant.
  • The aggregate gross proceeds from this offering are expected to be approximately $130 million.
  • The company also granted the underwriters a 30-day option to purchase up to 2,294,117 additional common shares.
  • The pre-funded warrants have an exercise price of $0.0001 per share and can be exercised at any time until fully exercised.
  • The offering was expected to close on or about November 14, 2025.
Nov 14, 2025, 9:39 PM
enGene Holdings Inc. Provides Update on Detalimogene Voraplasmid Clinical Program and 2027 Approval Target
ENGN
Product Launch
New Projects/Investments
Guidance Update
  • enGene Holdings Inc. is developing detalimogene voraplasmid, a non-viral gene therapy targeting non-muscle invasive bladder cancer (NMIBC), a condition affecting approximately 730,000 patients in the US.
  • The pivotal cohort of the LEGEND program for BCG-unresponsive NMIBC patients with CIS has completed enrollment of 125 patients.
  • Clinical data from post-amendment patients shows a 63% anytime complete response rate (in 62 patients) and a 62% six-month complete response rate, indicating competitive efficacy compared to other approved products.
  • The product demonstrates a strong tolerability profile with a 42% treatment-related adverse event rate and low rates of dose interruptions (1.6%) and discontinuations (0.8%), which is notably better than other agents.
  • Detalimogene voraplasmid offers logistical advantages due to its non-viral nature, simplifying storage and administration for community urologists. The company projects a potential FDA approval in 2027 and has sufficient cash to operate until then.
Nov 12, 2025, 7:00 PM