Phase 1a/b Tolerability of NTR-1011 in Healthy Adults and Adult Patients With SLE and RA

NCT ID
NCT07237659
Registry status
Recruiting
Study type
Interventional
Phase
Phase 1
Sponsor
Neutrolis
Conditions
RA - Rheumatoid Arthritis, SLE (Systemic Lupus)

Overview

ClinicalTrials.gov lists this study as Recruiting.

Official title: A Phase 1a/b, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety of NTR-1011 in Healthy Adults and Adult Patients With Systemic Lupus Erythematosus (SLE) and Rheumatoid Arthritis (RA)

Enrollment: 24 participants (Estimated).

What is being studied

  • Drug: NTR1011

Who may be eligible

Ages
18 Years to 75 Years
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Phase 1a - Healthy Volunteers (Completed, No Longer Enrolling) Key Inclusion Criteria * Healthy men and women, 18-55 years of age * Body mass index (BMI) between 17.0 and 30.0 kg/m² * Good general health, confirmed by medical history, physical exam, vital signs, ECG, and lab testing * Willing and able to use highly effective contraception during and after the study Key Exclusion Criteria * Pregnant or breastfeeding * History of drug allergies or anaphylaxis to human, murine, or yeast proteins, monoclonal antibodies, or other allergens * Use of an investigational drug within 30 days (or 5 half-lives) before dosing * Positive test for hepatitis B, hepatitis C, or HIV * Clinically significant heart, lung, digestive, blood, autoimmune, psychiatric, or other medical condition * Clinically significant abnormal lab values (e.g., liver enzymes, blood counts) or ECG findings * Uncontrolled high blood pressure * Poor venous access Phase 1b - Adult Patients with SLE and RA (Actively Recruiting) General Inclusion Criteria (All Patients) * Men and women, 18-75 years of age * Able to understand and sign informed consent, and comply with study visits * Willing and able to use highly effective contraception during and after the study Additional Inclusion Criteria - SLE Patients * Diagnosis of SLE for at least 6 months, meeting 2019 EULAR/ACR classification criteria * Active disease at screening * Positive lupus-related antibodies (e.g., anti-dsDNA, anti-Smith) and low complement (C3/C4) * On stable standard-of-care background therapy (e.g., antimalarials, low-dose corticosteroids, and at least one conventional DMARD) * Up to date on age-appropriate vaccinations Additional Inclusion Criteria - RA Patients * Diagnosis of RA for at least 3 months, meeting 2010 ACR/EULAR classification criteria * Moderate-to-severe active disease * Seropositive for rheumatoid factor and/or anti-CCP antibodies * On stable standard-of-care background therapy (e.g., low-dose corticosteroids and at least one conventional DMARD) Key Exclusion Criteria (All Patients) * Pregnant or breastfeeding * Known allergy or reaction to NTR-1011, placebo components, or related products * Use of an investigational drug within 30 days (or 5 half-lives) before dosing, or concurrent enrollment in another clinical trial * History of cancer within the past year (with limited exceptions) * Significant kidney impairment, severe liver dysfunction, or severe lung disease * Uncontrolled high blood pressure or significant cardiovascular disease (e.g., recent heart attack or stroke, certain arrhythmias) * Active, recurrent, or high-risk infection, including active or latent tuberculosis without appropriate treatment, opportunistic infections, or chronic hepatitis B * Recent symptoms of COVID-19 without a documented negative test * Receipt of a live vaccine within 4 weeks before screening or planned within 4 weeks after last dose * Significant central nervous system disease or pain-amplification conditions (e.g., epilepsy, fibromyalgia) that could interfere with study assessments * Major surgery within 8 weeks before screening or planned within 6 months after baseline * History of bone marrow, stem cell, or solid organ transplant (except cornea) * Uncontrolled diabetes within the past 12 months (with some exceptions) * History of a blood clot within the past 12 months (with some exceptions) * Clinically significant abnormal lab values (e.g., liver enzymes, blood counts) at screening

Study locations

7 study locations are listed.

Recruiting site status is explicitly provided for 7 locations; 7 are listed as Recruiting.

Countries: United States

  • California, United States: 7

Sample of listed locations

  • Carewell Arthritis Center — Apple Valley, California, 92307, United States — Recruiting
  • Attune Health Research Inc — Beverly Hills, California, 90211, United States — Recruiting
  • Covina Arthritis Clinic — Covina, California, 91722, United States — Recruiting
  • Novamed — Monterey Park, California, 91752, United States — Recruiting
  • Southland Arthritis Clinic — Riverside, California, 92508, United States — Recruiting
  • Southland Arthritis Clinic — Temecula, California, 92592, United States — Recruiting
  • Foothill Arthritis Clinic — Tujunga, California, 91042, United States — Recruiting

Study details

Start date
July 15, 2026
Primary completion date
March 31, 2027
Completion date
August 31, 2027
First posted
November 20, 2025

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07237659
Registry last updated
July 20, 2026
QualifiedStudies registry data refreshed
October 2, 2026
QualifiedStudies record fetched
October 2, 2026

View NCT07237659 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

About joining clinical research

Find clinical trials you may match with

QualifiedStudies can help you search for research opportunities related to your health. Availability of this specific study through QualifiedStudies has not been established.

Find clinical trials you may match with | Clinical trial FAQ