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A Single and Multiple Ascending Dose Study of LAD603 in Healthy Subjects

← catalyst calendar

NCT06200597

Sponsored by Almirall, S.A. (industry) · ALM.MC — their whole pipeline →.

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
92actual
Sites
1
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-12-05actualWhen the study began enrolling
Primary completion2025-05-11actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-05-29actualThe whole study's end, after follow-up
First posted2024-01-11actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-12-17actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Healthy Volunteers

Interventions

  • Drug: LAD603
  • Other: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Part 1: Number of Participants with Adverse Events (AEs) and Severity of AEs
measured Baseline up to Day 31
Part 1: Number of Participants with Clinically Significant Changes from Baseline in Vital Sign Parameter
measured Baseline up to Day 31
Part 1: Number of Participants with Clinically Significant Changes from Baseline in Electrocardiograms (ECGs) Parameters
measured Baseline up to Day 31
Part 1: Number of Participants with Clinically Significant Changes from Baseline in Clinical Laboratory Parameters
measured Baseline up to Day 31
Part 2: Number of Participants with AEs and Severity of AEs
measured Baseline up to Day 64
Part 2: Number of Participants with Clinically Significant Changes from Baseline in Vital Sign Parameter
measured Baseline up to Day 64
Part 2: Number of Participants with Clinically Significant Changes from Baseline in ECGs Parameters
measured Baseline up to Day 64
Part 2: Number of Participants with Clinically Significant Changes from Baseline in Clinical Laboratory Parameters
measured Baseline up to Day 64

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