Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

New cheaper insulin on the horizon? biosimilar I004 tested against NovoLog

NCT ID NCT07560150

First seen May 02, 2026 · Last updated Jun 23, 2026 · Updated 9 times

Summary

This study compares a new rapid-acting insulin called I004 to the approved insulin NovoLog in 60 healthy adults. Researchers want to see if the two insulins are similar in how they work in the body. If they are, I004 could become a more affordable option for managing diabetes.

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 PHARMACODYNAMICS are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Amphastar Study Site

    RECRUITING

    Chula Vista, California, 91911, United States

    Contact Phone: •••-•••-•••• Email: •••••@•••••

What this could mean

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

Active substance

Insulin aspart (a rapid-acting insulin analogue)

What this could lead to

If successful, this could lead to a more affordable biosimilar insulin for people with diabetes, helping to lower treatment costs.

What could go wrong

This is an early-stage study in healthy volunteers, not people with diabetes. It only measures short-term effects, so it may not predict real-world outcomes or long-term safety.

As listed by the trial registrant

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