Experimental biologic CND319 takes first steps toward taming autoimmune diseases
NCT ID NCT07712939
First seen Jul 20, 2026 · Last updated Jul 23, 2026 · Updated 3 times
Summary
This early-stage study tests an experimental drug called CND319 in healthy volunteers and people with rheumatoid arthritis or Sjögren's syndrome. The main goal is to check safety and how the body processes the drug. Researchers will also look for early signs that it might help control these autoimmune conditions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- an experimental biologic drug called CND319
- What this could lead to
- If successful, this could lead to a new treatment option for rheumatoid arthritis and Sjögren's syndrome.
- What could go wrong
- This is an early, first-in-human trial focused on safety, so the drug may not prove effective or could have unexpected side effects.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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About 105 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2028
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria (SAD): 1. 18 to 65 years old 2. Body mass index 18-30 kg/m2 and weight 55-100 kg 3. Individuals in good health 4. Agree to abstain from consumption of alcohol 48 hours prior to study visits 5. Agree to the use of highly effective contraception as defined in the protocol Inclusion Criteria (MAD and Part 2 Expansion): Patients with RA: 1. 18 to 75 years old 2. Diagnosis of adult-onset RA 3. Class I-III RA 4. Moderately to severely active RA Patients with SjD: 1. 18 to 75 years old 2. Diagnosis of primary SjD Exclusion Criteria (SAD): 1. Inadequate clinical laboratory parameters at Screening 2. Active infection 3. Receipt of or inability to discontinue any excluded therapies 4. Individuals with immediate household contact with your children (eg, ≤ 6 years old) or immunocompromised persons 5. History of alcohol or drug abuse within last 12 months 6. Positive alcohol breathalyzer or drug screen prior to dosing 7. Inability to comply with protocol-mandated requirements 8. History of severe allergic or anaphylactic reactions to mAb therapy (or recombinant anti-body-related fusion proteins) or any constituents of study drug 9. Major surgery requiring use of general anesthesia within 12 weeks or planned or expected major surgery during the study 10. Blood donation or significant blood loss within 30 days 11. Individuals considered to be part of a vulnerable population (eg, incarceration) 12. Individuals that in the opinion of the Investigator, are not suitable for participation in the trial Exclusion Criteria for patients with RA or SjD: 1. Inadequate clinical laboratory parameters at Screening 2. Active infection 3. Receipt of or inability to discontinue any excluded therapies 4. History of progressive multifocal leukoencephalopathy 5. Central nervous system disease 6. Presence of 1 or more significant concurrent medical conditions 7. Have a diagnosis or history of malignant disease within 5 years 8. History of severe allergic or anaphylactic reactions to mAb therapy (or recombinant antibody-related fusion proteins) or any constituents of study drug 9. Women who are pregnant or breastfeeding 10. Patients who do not agree to the use of highly effective contraception as defined by the protocol
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Candid Clinical Site
RECRUITINGMelbourne, Victoria, Australia
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Hidden kidney damage may lurk in rheumatoid arthritis patients
- Can a new injection calm rheumatoid arthritis? an early trial puts ZB002 to the test
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- Can a new biologic ease rheumatoid arthritis when standard drugs fail?
- A blood marker may reveal hidden heart risk in rheumatoid arthritis