New hope for rare amyloidosis: targeted drug combo enters trial

NCT ID NCT07335887

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

Summary

This phase 2 trial tests a drug called sonrotoclax, combined with dexamethasone and sometimes daratumumab, in 39 people with a specific genetic form of AL amyloidosis (t(11;14)). The goal is to see if the treatment can quickly reduce harmful protein levels and improve organ function. Participants will receive the therapy for 12 cycles, and researchers will monitor response rates and safety.

What this could mean

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

Active substance

Sonrotoclax (a targeted drug) plus dexamethasone, with or without daratumumab

What this could lead to

If successful, this could offer a new treatment option for people with a specific genetic type of AL amyloidosis, potentially improving organ function and survival.

What could go wrong

This is a small, early-phase trial with only 39 participants, so results may not apply broadly. The drug may cause side effects or fail to improve outcomes.

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.

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Conditions

The condition(s) this trial relates to.

AL amyloidosis Immunoglobulin Light-chain Amyloidosis primary systemic amyloidosis

As listed by the trial registrant

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