A Study of LAD106 in Healthy Adult Participants
Recruiting now · Phase 1 · Has a placebo group
Conditions studied: Healthy Volunteers
In brief
The main aim of this study is to assess the safety, tolerability, pharmacokinetics (PK), immunogenicity and pharmacodynamics (PD) of single ascending doses of LAD106 (Part A) and multiple ascending doses of LAD106 (Part B) in human healthy participants.
Key facts
- Study ID
- NCT07471932
- Run by
- Almirall, S.A.
- People needed
- 93
- Starts
- 2026-02-17
- Expected to finish
- 2027-05-31
- Last updated by the study team
- 2026-05-15
Who can join
Age: 18 and older, up to 45. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Signed informed consent and willing and able to comply with the study protocol.
- Healthy men or women,18 to 45 years of age (inclusive) at screening.
- Female participants agree to use effective contraception.
- Male volunteers agree to use barrier protection when they engage in sexual relations with women of child-bearing potential (WOCBP) or lactating women.
- Body mass index (BMI) between 18 and 32 kilograms per square meter (kg/m\^2), inclusive, and with a minimum bodyweight of 50 kg.
- Has the ability to communicate well with the Investigator in Dutch language and willing to comply with the study restrictions.
You may not qualify if…
- Evidence of any active or chronic disease or condition that could interfere with, or for which the treatment of might interfere with, the conduct of the study, or that would pose an unacceptable risk to the participant in the opinion of the investigator.
- Clinically significant abnormalities, as judged by the Investigator, in laboratory test results.
- Use of any medications (prescription or over-the-counter [OTC]), within 14 days prior to IMP dosing or less than 5 half-lives (whichever is longer). An exception is made for paracetamol (up to 4 g/day).
- If a woman, pregnant, or breast-feeding, or planning to become pregnant during the study.
Where it is running
- Centre for Human Drug Research (CHDR) Phase 1 Unit — Leiden, Netherlands (enrolling)
Full record on ClinicalTrials.gov
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