Autopsy report · NCT06622668
NTLA-3001 in Adults with Alpha-1 Antitrypsin Deficiency-Associated Lung Disease
Cause of deathFunding or business
“Clinical trial ITL-3001-CL-101 for the investigational product NTLA-3001 was withdrawn due to prioritization of other Sponsor programs.”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Phase 1, Phase 2
- Sponsor
- Intellia Therapeutics
- Sponsor type
- Industry
- Conditions
- Lung Disease; Pulmonary Disease; AATD; Alpha-1 Antitrypsin Deficiency; Alpha-1 Antitrypsin Deficiency-associated Lung Disease
- Interventions
- Biological NTLA-3001
- Participants
- 0
- Sites
- 1
- Countries
- New Zealand
Trials that died the same way
- Phase 3 Trial to Evaluate the Efficacy and Safety of DKP21102_B Added on to DKP21102_A Compared With DKP21102_A
“The clinical trial was withdrawn due to a commercial decision.” - A Study to Evaluate the Efficacy and Safety of REL-1017 As Adjunctive Treatment of Major Depressive Disorder (MDD)
“The study was withdrawn based on business-related matters and there are no new safety concerns related to the trial. No patients were enrolled.” - Medication Use Among American Indians Adults
“The study has not been stopped. The study does not qualify as a clinical trial so it was withdrawn from clinicaltrials.gov.” - PD-1, LAG-3 and TIM-3 Checkpoint Blockade in DLBCL
“Investigator request to no longer pursue this study. Lack of support from drug company. This trial never opened. Withdrew IND.” - A Dose-ranging Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Low Back Pain
“Based on lack of efficacy in PAI2003, sponsor made the decision to discontinue the trial.”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.