Chirens, France
Safety and Efficacy of Intravenous Thrombolysis in Patients With Ischemic Stroke and Direct Oral Anticoagulants Intake
Phase
4Span
216 weeksSponsor
Insel Gruppe AG, University Hospital BernChristchurch
Recruiting
A Study to Evaluate KRIYA-825 (VV-14295) in Adults with Geographic Atrophy Secondary to Age-related Macular Degeneration
Phase
1/2Span
146 weeksSponsor
Kriya Therapeutics, Inc.Christchurch
Recruiting
Efficacy Study of EVO301 in Moderate to Severe Atopic Dermatitis
This is a Phase 2a efficacy and safety study of intravenous EVO301 in adults with moderate to severe atopic dermatitis.
Phase
2Span
51 weeksSponsor
Evommune, Inc.Christchurch
Recruiting
Study of ARO-ATXN2 Injection in Adults With Spinocerebellar Ataxia Type 2
Phase
1Span
94 weeksSponsor
Arrowhead PharmaceuticalsChristchurch
Recruiting
A Phase 1/2a, Single- and Multiple-dose Escalation Study of KRRO-110
Phase
1/2Span
103 weeksSponsor
Korro Bio, Inc.Christchurch
Recruiting
Healthy Volunteers
A Study to Assess the Safety, Pharmacokinetics, and Tolerability of ABI-1179 in Healthy Subjects and in Subjects Seropositive for HSV-2 With Recurrent Genital Herpes
Phase
1Span
56 weeksSponsor
Assembly BiosciencesChristchurch
Recruiting
Healthy Volunteers
A Study of TX000045 in Patients With Pulmonary Hypertension Secondary to Heart Failure With Preserved Ejection Fraction (the APEX Study)
This study will enroll approximately 180 participants and eligible patients will be randomized to one of 3 treatment arms: - Arm 1: Treatment Group 1: Placebo delivered subcutaneously (SC) every 2 weeks (Q2W) for 24 weeks - Arm 2: Treatment Group 2: TX000045 SC at Dose A Q2W for 24 weeks - Arm 3: Treatment Group 3: TX000045 SC at Dose B Q2W alternating with Placebo Q2W for 24 weeks
Phase
2Span
111 weeksSponsor
Tectonic TherapeuticChristchurch
Recruiting
A Study of DR-01 in Subjects With Alopecia Areata and Vitiligo
Phase
1Span
100 weeksSponsor
Dren BioChristchurch
Recruiting
A Study to Evaluate Single-dose of HB0056 in Healthy Adult Participants
This is a single-dose escalation study of HB0056 to evaluate the safety, tolerability, pharmacokinetics, and immunogenicity of HB0056.
Phase
1Span
46 weeksSponsor
Shanghai Huaota Biopharmaceutical Co., Ltd.Christchurch
Recruiting
Healthy Volunteers
A Study Investigating the Efficacy and Safety of Intravitreal (IVT) Injections of ANX007 in Participants With Geographic Atrophy (GA)
Phase
3Span
170 weeksSponsor
Annexon, Inc.Christchurch, Canterbury
Recruiting