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Study identifier: NCT07421778 Synced from ClinicalTrials.gov · August 09, 2026
● Study status: Recruiting

A Multiple Ascending Dose Study Evaluating the Safety and Tolerability of a Novel Formulation of QRL-101 in Healthy Participants

Condition: Healthy Participant Study  ·  Sponsor: QurAlis Corporation

PhasePhase 1
Planned participants48
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersYesCheck eligibility criteria ↓
WhereGroningen, Netherlands

Interested? Contact the study team ↓

For sponsors, CROs & site teams
Professional view of this study — listed sites, countries and recruiting context from the public registry. Everything below is written for patients and caregivers.See where this study is running →

About this study

QRL-101-08 is a multiple ascending dose (MAD) study to evaluate the safety, tolerability, and pharmacokinetics (PK) of a novel formulation of QRL-101 in healthy participants.

This description comes directly from the study's public registry record.

Talk to the study team

QurAlis Corporation  ·  617-720-9566  ·  clinicaltrials@quralis.com

Salah Hadi, MD

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: 1. Age 18 to 65 years of age inclusive at the time of signing the informed consent. 2. Clinical chemistry laboratory values within acceptable range for the population, as per investigator judgment. 3. Body mass index of 18 to 32 kg/m2 (inclusive). 4. Willing and able to practice effective contraception. Exclusion Criteria: 1. Currently enrolled in any other clinical trial involving a study drug or off-label use of a drug or device, or any other type of medical research judged not to be scientifically or medically compatible with this study. 2. Any participant in \>4 studies a year and/or has participated in a clinical trial within 1 month of the expected dosing date. 3. History or presence of medical illness including, but not limited to, any cardiovascular, hepatic, respiratory, hematological, endocrine, psychiatric, or neurological disease, convulsions, or any clinically significant laboratory abnormality that, in the judgment of the investigator, indicate a medical problem that would preclude study participation.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (1)

ICON plc.Groningen, NetherlandsRecruiting

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Groningen

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