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Clinical Trials in the EU / 2026-526293-16-00
Authorised, recruiting Phase I

GRT-2U101: A randomized, double-blind, placebo-controlled single and multiple ascending dose study to evaluate safety, tolerability, and pharmacokinetics/pharmacodynamics of GRT-002 in healthy volunteers and patients with chronic spontaneous urticaria after single or multiple intravenous or subcutaneous dosing of GRT-002 (BASALT trial).

2026-526293-16-00 · tracked via the Priya Life Science EU tracker
Sponsor
Granite Bio AG
Sponsor type
Pharmaceutical company
Therapeutic area
Skin and Connective Tissue Diseases
Decision date
09/09/2026
Enrollment target
73
Sites
Germany

Condition studied

Chronic Spontaneous Urticaria

Eligibility

Age group
65+ years, 18-64 years
Sex
Female, Male
Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2026-526293-16-00 on CTIS ↗ ← All trials in the EU