Could less be more? kidney transplant study tests lower drug dose to save kidney function

NCT ID NCT00213590

First seen Jun 08, 2026 · Last updated Jun 19, 2026 · Updated 1 time

Summary

This study tested whether giving kidney transplant patients a lower dose of the anti-rejection drug cyclosporine A (combined with another drug, mycophenolate mofetil) could better protect their kidney function over time. The trial involved 208 adults who were at least one year post-transplant and had stable kidney function. Researchers measured kidney function after two years to see if the lower dose helped prevent further kidney damage.

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 KIDNEY FAILURE are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

Contacts and locations

Locations

  • CHU de ROUEN

    Rouen, 76031, France

What this could mean

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

Active substance

cyclosporine A (a drug that suppresses the immune system to prevent organ rejection)

What this could lead to

If successful, this could show that using less cyclosporine A helps protect kidney function in transplant recipients while still preventing rejection.

What could go wrong

This is a completed phase 3 trial, so results are available but may not apply to all patients. Lowering immunosuppression always carries a risk of organ rejection.

Conditions

The condition(s) this trial relates to.

Renal Insufficiency

As listed by the trial registrant

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