ClinicalTrials.gg
Active, not recruitingNCT07059312Updated Dec 18, 2025

A Phase 1 Study of JADE101 in Healthy Participants

A Phase 1 interventional study of JADE101 and Placebo in Healthy Volunteers, sponsored by Jade Biosciences, Inc.. Active, not recruiting at 1 site in New Zealand. Open to participants aged 18 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-12-18.

Sponsored by Jade Biosciences, Inc. · Phase 1, Interventional, and Basic science

Phase
Phase 1
Study type
Interventional
Enrollment
32
Allocation
Randomized
Ages
18 Years to 55 Years
Sex
All
01

Study summary

This is a Phase 1, first-in-human study to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of single ascending doses of JADE101 compared to placebo in healthy participants.

Read the detailed description

This is a single center, Phase 1, double-blind, placebo-controlled, randomized, first-in-human (FIH), single ascending dose study evaluating the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of JADE101 in healthy participants. The study will enroll approximately 32 healthy volunteers. JADE101 will be administered by a subcutaneous injection. The results of this study will help inform the dosing and frequency of dosing in future studies of JADE101.

02

Conditions studied

  • Healthy Volunteers

Keywords

  • JADE101
03

In context

Lead sponsor

Jade Biosciences, Inc. is the lead sponsor of 5 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Healthy male or female participants 18-55 years of age, inclusive
  2. A body weight between 50-100 kg and a (BMI) between 18.0 - 32.0 kg/m2 (all inclusive) at screening
  3. Willing and able to comply with the study site stay, scheduled visits, and study procedures
  4. Willing and able to comply with using two methods of (one being highly effective) and lifestyle requirements from admission through the end of the study

Exclusion criteria

Exclusion Criteria:

  1. Harmful alcohol use
  2. Smoking/vaping or heavy tobacco use within 2 years prior to screening
  3. Known history of abuse of illicit drugs
  4. Nursing, lactating or pregnant, or who have plans to become pregnant during the study
  5. Known history of disease
  6. Known history of immunodeficiency disorder
  7. History of clinically significant allergic reactions or
Terms in these criteria, in plain language(4)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

05

Study design

Phase
Phase 1
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Sequential assignment
Masking
Double (Participant, Investigator)
Enrollment
32 participants (actual)

Study arms

  • Experimental
    JADE101

    Subcutaneous (SC) injection of JADE101

    Drug: JADE101

  • Placebo comparator
    Placebo

    Subcutaneous (SC) injection of placebo

    Drug: Placebo

Interventions

  • JADE101 is supplied as sterile solution to be administered by SC injection.

  • DrugPlacebo

    Placebo solution to be administered at a matching volume by SC injection.

06

What researchers measure

Primary outcomes

  1. Safety and Tolerability of Single Ascending Doses of JADE101 in Healthy Participants

    Incidence of treatment-emergent adverse events

    Time frame: Day 1 through 48 weeks

Secondary outcomes

  1. Cmax

    Maximum observed serum concentration

    Time frame: Day 1 through 48 weeks

  2. Tmax

    Time to reach Cmax

    Time frame: Day 1 through 48 weeks

  3. AUClast

    The area under the concentration-time curve from time zero to the time of the last observed quantifiable (non-zero) concentration

    Time frame: Day 1 through 48 weeks

  4. T1/2

    Apparent first-order terminal elimination half-life

    Time frame: Day 1 through 48 weeks

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 18, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07059312
Lead sponsor
Jade Biosciences, Inc.
Responsible party
Sponsor
First posted
Jul 10, 2025
Start date
Aug 17, 2025
Primary completion
Oct 2026 (estimated)
Completion
Oct 2026 (estimated)
Last update
Dec 18, 2025

Study contacts

Li Li, MD
study director · Jade Biosciences, Inc.

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Dec 2025. You cannot join it, but the record below documents what was studied.

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Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

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Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Studies of the drug tested here: JADE101

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