Experimental interferon boosts hopes for rectal cancer remission

NCT ID NCT07662278

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This phase 2 trial tests whether adding a new form of interferon (rSIFN-co) to standard total neoadjuvant therapy (short-course radiation plus chemotherapy) can improve the chance of complete tumor disappearance in people with mid-low locally advanced rectal cancer. About 90 adults with this cancer will be randomly assigned to receive either the standard therapy alone or the standard therapy plus rectal interferon twice a week. The main goal is to see if more patients achieve a complete response (no cancer detectable after treatment).

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

recombinant super-compound interferon (rSIFN-co)

What this could lead to

If successful, this combination could increase the chance of eliminating all signs of rectal cancer before surgery, potentially reducing the need for more aggressive treatments.

What could go wrong

This is an early phase 2 trial with only 90 participants, so results may not apply to everyone. The added interferon may cause side effects and the complete response benefit is not guaranteed.

Disclaimer Read more

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for MID-LOW LOCALLY ADVANCED RECTAL CANCER are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

Conditions

The condition(s) this trial relates to.

rectal cancer

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.