Immutep's Efti Clinical Trial Shows Promising Survival Rates

Promising Results from the INSIGHT-003 Trial of Efti

The INSIGHT-003 trial has once again highlighted the potential of efti, a groundbreaking therapy developed by Immutep Limited (NASDAQ: IMMP), in the fight against non-small cell lung cancer (NSCLC). In this trial, patients displayed exceptional survival rates which surpass traditional benchmarks. With a minimum follow-up period of 22 months for 21 patients, the data suggests a transformative impact on treatment outcomes for this challenging disease.

Exceptional Survival Statistics

The trial results illuminate a median overall survival (OS) of 32.9 months. This figure stands in stark contrast to historical control data and shows the promise of efti in combination with KEYTRUDA® (pembrolizumab) and chemotherapy. Moreover, the median progression-free survival (PFS) reached 12.7 months, and the overall survival rate after 24 months is reported at 81.0%. These milestones showcase the efficacy of this innovative treatment approach.

Insighful Data Comparisons

Further comparisons reveal the marked improvement in overall response rates (ORR) across various patient groups. The participant pool in this study included 40 evaluable patients, illustrating significant enhancements in ORR compared to previous trials. In patients with high PD-L1 expression, the ORR climbed to 75.0%, compared to 62.1% registered in historical controls. This indicates that efti is effectively enhancing patient outcomes across a spectrum of PD-L1 expressions.

Safety Profile Remains Favorable

Importantly, the safety profile of efti when combined with pembrolizumab and chemotherapy has remained strong with no new safety signals arising. The trial continues to build confidence in the safety and tolerability of this treatment regimen, making it a promising option for patients with advanced NSCLC.

Future Perspectives and Upcoming Trials

As the INSIGHT-003 trial approaches the completion of patient enrollment, the excitement within the Immutep community grows. The company, led by CEO Marc Voigt, is optimistic about these results paving the way for further studies. The upcoming TACTI-004 Phase III trial aims to expand upon the findings of INSIGHT-003 and further validate the role of efti in standard oncology practice.

Expert Opinions on the Findings

Prof. Dr. Salah-Eddin Al-Batran from the Frankfurt Institute of Clinical Cancer Research (IKF), who leads the INSIGHT-003 trial, expressed optimism regarding the robust survival data combined with its safety profile. This combination of factors reinforces the hope that efti can contribute positively to the treatment landscape of non-squamous NSCLC.

About Immutep and Its Vision

Immutep Limited is recognized as a pioneering entity in the biopharmaceutical industry, focusing on LAG-3 immunotherapy for cancer and autoimmune diseases. The company continuously strives to harness its innovative technologies to provide new treatment options that enhance patient lives. As they explore efti's potential, they remain committed to establishing new standards of care across various cancers.

Company Contact Information

For Australian investors and media, please reach out to Catherine Strong at Sodali & Co., contactable via phone at +61 (0)406 759 268 or email at catherine.strong@sodali.com. For U.S. media inquiries, Chris Basta, VP of Investor Relations and Corporate Communications, is available at +1 (631) 318 4000 or chris.basta@immutep.com.

Frequently Asked Questions

What is the INSIGHT-003 trial about?

The INSIGHT-003 trial is an investigator-initiated study evaluating the effectiveness of efti in combination with KEYTRUDA and chemotherapy for first-line treatment of metastatic non-squamous NSCLC patients.

What were the key results of the trial?

The trial showed a median overall survival of 32.9 months, with significant improvements in progression-free survival and overall response rates when compared to historical controls.

How does efti perform in terms of safety?

The safety profile of efti remains favorable, with no new safety signals detected throughout the course of the trial.

What does the future hold for Immutep?

Immutep is preparing for the upcoming TACTI-004 Phase III trial, which aims to build on the promising results of INSIGHT-003 and validate the role of efti in treating NSCLC.

Who can be contacted for more information about Immutep?

For inquiries, Australian investors can contact Catherine Strong, while U.S. media inquiries can be directed to Chris Basta.

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