Replimune Reports Landmark Three-Year Survival Data
Written by Emily J. Thompson, Senior Investment Analyst
Updated: 13 hours ago
0mins
Source: NASDAQ.COM
- Clinical Trial Results: Replimune presented three-year survival data from its IGNYTE trial at the 2026 ASCO annual meeting, revealing that nearly half of treated patients were alive at three years, underscoring the durability and effectiveness of the treatment.
- Survival and Response Rates: The combination therapy achieved a median overall survival of 32.9 months, with an objective response rate of 33.6% and a median duration of response of 24.8 months, indicating that almost 45% of responders maintained their response at three years, showcasing broad applicability among patients.
- Safety Profile Analysis: The regimen demonstrated consistent survival benefits across key patient subgroups and maintained a favorable safety profile, primarily consisting of Grade 1-2 side effects with no new safety signals, further enhancing its clinical application potential.
- Company Development Strategy: Founded in 2015, Replimune is advancing its RPx platform to develop versatile oncolytic immunotherapies that can be used alone or in combination with other treatments, marking significant innovation progress in the field of cancer therapy.
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Analyst Views on REPL
Wall Street analysts forecast REPL stock price to rise
7 Analyst Rating
4 Buy
3 Hold
0 Sell
Moderate Buy
Current: 4.680
Low
3.00
Averages
11.43
High
18.00
Current: 4.680
Low
3.00
Averages
11.43
High
18.00
About REPL
Replimune Group, Inc. is a clinical-stage biotechnology company engaged in the development of novel oncolytic immunotherapies. Its proprietary RPx platform is based on a potent HSV-1 backbone intended to maximize immunogenic cell death and the induction of a systemic anti-tumor immune response. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor-derived antigens and altering of the tumor microenvironment to ignite a systemic response. Its lead product candidate, RP1, is a selectively replicating version of HSV-1 that expresses GALV-GP R(-) and human GM-CSF. Its lead indication for its lead product candidate, RP1, is the potential treatment of advanced melanoma. Its pipeline product candidates include RP2 and RP3. It has designed its RP2 product candidate to express an anti-CTLA-4 antibody-like protein intended to block the inhibition of the immune response.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
Replimune Reports Landmark Three-Year Survival Data
- Clinical Trial Results: Replimune presented three-year survival data from its IGNYTE trial at the 2026 ASCO annual meeting, revealing that nearly half of treated patients were alive at three years, underscoring the durability and effectiveness of the treatment.
- Survival and Response Rates: The combination therapy achieved a median overall survival of 32.9 months, with an objective response rate of 33.6% and a median duration of response of 24.8 months, indicating that almost 45% of responders maintained their response at three years, showcasing broad applicability among patients.
- Safety Profile Analysis: The regimen demonstrated consistent survival benefits across key patient subgroups and maintained a favorable safety profile, primarily consisting of Grade 1-2 side effects with no new safety signals, further enhancing its clinical application potential.
- Company Development Strategy: Founded in 2015, Replimune is advancing its RPx platform to develop versatile oncolytic immunotherapies that can be used alone or in combination with other treatments, marking significant innovation progress in the field of cancer therapy.
See More
Replimune Secures FDA Approval to Resubmit RP1 Application
- FDA Resubmission: Replimune successfully convinced the FDA to reconsider its Biologics License Application for RP1, despite two prior rejections, thanks to intervention from White House officials, highlighting government concern for terminally ill patients.
- Positive Market Reaction: Following the announcement of an agreement with the FDA to resubmit the RP1 application, Replimune's shares surged on Friday, reflecting increased investor confidence in the treatment, particularly in combination with Bristol Myers' nivolumab.
- New Data Submission: Replimune plans to present new data not previously shared with the FDA in its upcoming application, which could significantly influence the review outcome and provide new support for RP1's approval.
- Regulatory Investigation Findings: Although the White House requested an investigation into the previous rejections, the report found no procedural errors, indicating that the FDA's review process remains stringent, and Replimune must provide compelling evidence in its new application to secure approval.
See More
Replimune Secures FDA Agreement, Shares Surge 80%
- FDA Prioritization: Replimune has reached an agreement with the FDA to resubmit its Biologics License Application for RP1, with the FDA treating this as an urgent matter, highlighting the significant unmet needs of advanced melanoma patients and potentially accelerating the review process.
- Stock Surge: Following the agreement, Replimune's shares surged 80% on Friday, breaching the 200-day moving average and marking the largest single-day gain in over seven months, reflecting renewed investor optimism regarding the company's prospects.
- Regulatory Uncertainty: The FDA had previously rejected the application twice, leading CEO Sushil Patel to criticize the review process as inconsistent, which forced the company to cut jobs and scale back U.S. manufacturing operations, indicating the substantial impact of regulatory environments on business operations.
- Leadership Change Impact: The agreement comes after a leadership shakeup at the FDA, with former head Marty Makary stepping down, which has drawn widespread criticism regarding the agency's handling of drug reviews, further exacerbating industry concerns about delays in the approval of new treatments.
See More
Biotech Stocks Show Significant Pre-Market Activity
- Significant Pre-Market Gains: Replimune Group, Inc. (REPL) surged 69% to $7.92 in pre-market trading, indicating strong market confidence in its potential breakout, which may attract more investor interest.
- Other Gaining Stocks: aTyr Pharma, Inc. (ATYR) rose 15% to $0.56, while Basel Medical Group Ltd. (BMGL) and Artiva Biotherapeutics, Inc. (ARTV) both increased by 10% to $0.64 and $8.34 respectively, reflecting an overall positive sentiment in the biotech sector.
- Pre-Market Decliners: Rocket One Inc. (RKTO) fell 16% to $1.43 in pre-market trading, reflecting market concerns about its future performance, which may lead investors to reassess their investment strategies.
- Other Declining Stocks: SciSparc Ltd. (SPRC) dropped 13% to $9.15, and Aethlon Medical, Inc. (AEMD) decreased by 11% to $2.60, indicating challenges faced by some biotech companies that could impact market confidence.
See More
Replimune Plans to Resubmit Melanoma Drug Application to FDA
- FDA Resubmission: Replimune plans to resubmit its melanoma drug application following leadership changes at the FDA, after two previous rejections under former Commissioner Marty Makary, indicating improved alignment between the company and the agency that could offer new hope for patients.
- Positive Market Reaction: Following the announcement, Replimune's shares surged by 70% in premarket trading, reflecting investor optimism about the company's future prospects, with a market value of $386 million as of Thursday's close.
- Clinical Trial Controversy: Replimune accused the FDA of wrongfully blocking its drug, which is seen as a promising treatment for skin cancer, while the FDA claimed the company did not adhere to clinical trial guidelines, highlighting the complexities in the drug approval process.
- Significant Patient Impact: Replimune stated that the constructive dialogue with the FDA represents a crucial step forward for thousands of patients with advanced melanoma who have limited treatment options after prior anti-PD-1 therapies, underscoring the importance of new drug approvals in enhancing patient care.
See More
Replimune Plans to Resubmit Melanoma Drug Application Following FDA Leadership Change
- Resubmission Announcement: Replimune plans to resubmit its melanoma drug application under the new FDA leadership after two previous rejections under former Commissioner Marty Makary, indicating increased confidence in the agency's current direction.
- FDA Urgent Review: The FDA has indicated it will treat Replimune's application as urgent, which not only brings hope to the company but also to thousands of advanced melanoma patients with limited treatment options available.
- Positive Market Reaction: Following the announcement, Replimune's shares surged by 70% in premarket trading, reflecting investor optimism about the company's future prospects and boosting its market value to $386 million.
- Broader Industry Implications: The constructive dialogue between Replimune and the FDA is seen as a sign of improving relations between the pharmaceutical industry and regulators, potentially influencing the approval processes for other drugs and fostering the development of more innovative therapies.
See More
Replimune Reports Landmark Three-Year Survival Data
- Clinical Trial Results: Replimune presented three-year survival data from its IGNYTE trial at the 2026 ASCO annual meeting, revealing that nearly half of treated patients were alive at three years, underscoring the durability and effectiveness of the treatment.
- Survival and Response Rates: The combination therapy achieved a median overall survival of 32.9 months, with an objective response rate of 33.6% and a median duration of response of 24.8 months, indicating that almost 45% of responders maintained their response at three years, showcasing broad applicability among patients.
- Safety Profile Analysis: The regimen demonstrated consistent survival benefits across key patient subgroups and maintained a favorable safety profile, primarily consisting of Grade 1-2 side effects with no new safety signals, further enhancing its clinical application potential.
- Company Development Strategy: Founded in 2015, Replimune is advancing its RPx platform to develop versatile oncolytic immunotherapies that can be used alone or in combination with other treatments, marking significant innovation progress in the field of cancer therapy.
See More
Replimune Secures FDA Approval to Resubmit RP1 Application
- FDA Resubmission: Replimune successfully convinced the FDA to reconsider its Biologics License Application for RP1, despite two prior rejections, thanks to intervention from White House officials, highlighting government concern for terminally ill patients.
- Positive Market Reaction: Following the announcement of an agreement with the FDA to resubmit the RP1 application, Replimune's shares surged on Friday, reflecting increased investor confidence in the treatment, particularly in combination with Bristol Myers' nivolumab.
- New Data Submission: Replimune plans to present new data not previously shared with the FDA in its upcoming application, which could significantly influence the review outcome and provide new support for RP1's approval.
- Regulatory Investigation Findings: Although the White House requested an investigation into the previous rejections, the report found no procedural errors, indicating that the FDA's review process remains stringent, and Replimune must provide compelling evidence in its new application to secure approval.
See More
Replimune Secures FDA Agreement, Shares Surge 80%
- FDA Prioritization: Replimune has reached an agreement with the FDA to resubmit its Biologics License Application for RP1, with the FDA treating this as an urgent matter, highlighting the significant unmet needs of advanced melanoma patients and potentially accelerating the review process.
- Stock Surge: Following the agreement, Replimune's shares surged 80% on Friday, breaching the 200-day moving average and marking the largest single-day gain in over seven months, reflecting renewed investor optimism regarding the company's prospects.
- Regulatory Uncertainty: The FDA had previously rejected the application twice, leading CEO Sushil Patel to criticize the review process as inconsistent, which forced the company to cut jobs and scale back U.S. manufacturing operations, indicating the substantial impact of regulatory environments on business operations.
- Leadership Change Impact: The agreement comes after a leadership shakeup at the FDA, with former head Marty Makary stepping down, which has drawn widespread criticism regarding the agency's handling of drug reviews, further exacerbating industry concerns about delays in the approval of new treatments.
See More
Biotech Stocks Show Significant Pre-Market Activity
- Significant Pre-Market Gains: Replimune Group, Inc. (REPL) surged 69% to $7.92 in pre-market trading, indicating strong market confidence in its potential breakout, which may attract more investor interest.
- Other Gaining Stocks: aTyr Pharma, Inc. (ATYR) rose 15% to $0.56, while Basel Medical Group Ltd. (BMGL) and Artiva Biotherapeutics, Inc. (ARTV) both increased by 10% to $0.64 and $8.34 respectively, reflecting an overall positive sentiment in the biotech sector.
- Pre-Market Decliners: Rocket One Inc. (RKTO) fell 16% to $1.43 in pre-market trading, reflecting market concerns about its future performance, which may lead investors to reassess their investment strategies.
- Other Declining Stocks: SciSparc Ltd. (SPRC) dropped 13% to $9.15, and Aethlon Medical, Inc. (AEMD) decreased by 11% to $2.60, indicating challenges faced by some biotech companies that could impact market confidence.
See More
Replimune Plans to Resubmit Melanoma Drug Application to FDA
- FDA Resubmission: Replimune plans to resubmit its melanoma drug application following leadership changes at the FDA, after two previous rejections under former Commissioner Marty Makary, indicating improved alignment between the company and the agency that could offer new hope for patients.
- Positive Market Reaction: Following the announcement, Replimune's shares surged by 70% in premarket trading, reflecting investor optimism about the company's future prospects, with a market value of $386 million as of Thursday's close.
- Clinical Trial Controversy: Replimune accused the FDA of wrongfully blocking its drug, which is seen as a promising treatment for skin cancer, while the FDA claimed the company did not adhere to clinical trial guidelines, highlighting the complexities in the drug approval process.
- Significant Patient Impact: Replimune stated that the constructive dialogue with the FDA represents a crucial step forward for thousands of patients with advanced melanoma who have limited treatment options after prior anti-PD-1 therapies, underscoring the importance of new drug approvals in enhancing patient care.
See More
Replimune Plans to Resubmit Melanoma Drug Application Following FDA Leadership Change
- Resubmission Announcement: Replimune plans to resubmit its melanoma drug application under the new FDA leadership after two previous rejections under former Commissioner Marty Makary, indicating increased confidence in the agency's current direction.
- FDA Urgent Review: The FDA has indicated it will treat Replimune's application as urgent, which not only brings hope to the company but also to thousands of advanced melanoma patients with limited treatment options available.
- Positive Market Reaction: Following the announcement, Replimune's shares surged by 70% in premarket trading, reflecting investor optimism about the company's future prospects and boosting its market value to $386 million.
- Broader Industry Implications: The constructive dialogue between Replimune and the FDA is seen as a sign of improving relations between the pharmaceutical industry and regulators, potentially influencing the approval processes for other drugs and fostering the development of more innovative therapies.
See More
