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

Gå till den engelska sidan

Experimental KRRO-110 trial for rare lung condition halted early

NCT ID NCT06677307

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early This study
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

Summary

This study tested an experimental drug called KRRO-110 in healthy volunteers and people with Alpha-1 Antitrypsin Deficiency (AATD), a genetic condition that can cause lung and liver damage. The goal was to check safety and how the drug moves through the body. However, the trial was terminated before completion, so no final conclusions can be drawn.

What this could mean

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

Active substance
KRRO-110 (an experimental drug given intravenously)
What this could lead to
If successful, KRRO-110 could help control Alpha-1 Antitrypsin Deficiency by raising protective enzyme levels, potentially slowing lung damage.
What could go wrong
This early-stage trial was terminated, so results are unknown. The drug is first-in-human, meaning safety and effectiveness are not yet established.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 1/2

Runs two stages together: safety and dose first, then whether the treatment works.

Participants

42 people

The number who actually took part.

Started

Jan 2025

Finished

Dec 2025

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 70 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: Part A SAD cohort Inclusion Criteria (Healthy Volunteers) * Adult male or female participants, 18 to 65 years of age * Documented PiMM genotype * Participants who are willing to and able to provide signed written informed consent PiZZ Genotype (Part A SAD and Part B MAD cohorts) Inclusion Criteria (PiZZ Genotype) * Adult male or female participants 18 to 70 years of age (inclusive) * Documented PiZZ genotype * Baseline blood total AAT level \< 11 µM/L Exclusion Criteria: Exclusion Criteria (Healthy Volunteers) * Female participant of childbearing potential or male participant that is unable or unwilling to use an approved, reliable means of contraception * Body mass index (BMI) \> 32 or \< 18.5 kg/m2 * History or current clinical evidence of hepatic disease * Evidence of active infection * History of medical condition(s), eg, advance cardiac disease, current or recent malignancy, organ transplantation, or other illness * Serology result indicative of any exposure (past or active) to hepatitis C, hepatitis B, or human immunodeficiency virus (HIV) * Respiratory or other acute illness within 8 weeks * Tobacco use of any kind within 6 months Exclusion Criteria (PiZZ Genotype) * Female participant of childbearing potential or male participant that is unable or unwilling to use an approved, reliable means of contraception * BMI \> 32 or \< 18.5 kg/m2 or weight \> 90 kg * History of FEV1 \< 35% * History or current clinical evidence of advanced hepatic disease and/or pulmonary disease * Use of an experimental therapy except KRRO-110 within 6 months or 5 half-lives for the experimental therapy, whichever is greater * Tobacco use of any kind within 6 months * Use of conventionally dosed AAT augmentation therapy within 5 half-lives * Serology result consistent with exposure to HIV, or serology consistent with active hepatitis B or hepatitis C infection

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for AATD are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • New Zealand Clinical Research

    Auckland, New Zealand

  • New Zealand Clinical Research

    Christchurch, New Zealand

  • Nucleus Network Pty Ltd

    Melbourne, Victoria, 3004, Australia

  • St. Vincent's Hospital Melbourne

    Melbourne, Victoria, 3065, Australia

  • The Prince Charles Hospital

    Brisbane, Queensland, 4032, Australia

More trials for these conditions

Other studies related to the condition(s) this trial covers.