A Phase 1/2a, Single- and Multiple-dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacodynamics, and Pharmacokinetics of KRRO 110 in Healthy Adult Volunteers and in Adult Participants with Alpha-1 Antitrypsin Deficiency (AATD) (REWRITE)
Latest Information Update: 16 May 2025
At a glance
- Drugs KRRO 110 (Primary)
- Indications Alpha 1-antitrypsin deficiency
- Focus Adverse reactions; First in man
- Acronyms REWRITE
- Sponsors Korro Bio
Most Recent Events
- 07 May 2025 According to a Korro media release, the company received regulatory approval to expand the REWRITE clinical trial in New Zealand, and continues to progress enrollment, site activation and expansion into other geographies beyond Australia and New Zealand, including the United States.
- 18 Mar 2025 According to Korro Bio media release, company announced the completion of dosing of the first two single ascending dose cohorts in healthy adult volunteers in Phase 1/2a REWRITE clinical study of KRRO-110 and Interim readout expected in the second half of 2025.
- 13 Jan 2025 According to Korro Bio media release, company announced the initiation of dosing in this REWRITE study.