Improving Physical Function in Older Adults Using an Anti-inflammation Drug: The RIGHT Study

NCT ID: NCT05727384

Last Updated: 2025-12-19

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 29 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-08-01
• Study Completion Date: 2026-07-31

Brief Summary

The goal of this clinical trial is to learn about the effects of inflammation-lowering therapy on mobility and disability in older adults. The main questions it aims to answer are:

• Will therapy improve walking speed/pace?
• Will therapy improve levels of blood inflammation markers and other indicators of physical, cognitive and immune function?

Participants will be asked to receive injections of drug or placebo every 4 weeks for 24 weeks. They will also be asked to undergo testing that assesses physical function, thinking ability and brain health, breathing capacity, and blood vessel stiffness, and will have blood samples collected to measure immune function and to create a bank of samples for future testing. Comparisons will be made between those who receive drug and those who receive placebo.

Detailed Description

The primary objective of this trial is to assess the impact of inflammation-lowering therapy with clazakizumab 5 mg/month on speed when walking 400 meters in older adults. The investigators hypothesize that participants treated with clazakizumab will see a larger 6-month improvement in their pace on a 400-meter walk than those provided placebo.

The aims of the study will be to:

• To test the effect of clazakizumab 5 mg/month for 6 months on walking speed during a 400- meter corridor walk in adults 70 years of age and older with baseline levels of IL-6 ≥ 2.0 pg/ml and < 30 pg/ml
• To assess the effect of clazakizumab 5 mg/month on serum levels of free interleukin (IL-6), circulating C-reactive protein (CRP), and other inflammatory markers
• To assess the effect of clazakizumab 5 mg/month on oxygen utilization (VO2) during submaximal steady-state walking in adults 70 years of age and older with baseline levels of IL-6 ≥ 2.0 pg/ml and < 30 pg/ml, physical function, physical activity, perceived fatigability (overall, by questionnaire and in association with preferred and fixed speed walking), cognition, body weight, blood pressure, vascular stiffness, endothelial function, kidney function and immune function
• To determine the safety and tolerability of clazakizumab 5 mg/month

This study will randomize 60 community living men and women 70 years of age and older who have mildly elevated IL-6 at baseline (≥ 2.0 pg/ml and < 30.0 pg/ml). Interested individuals will undergo telephone and in-person screening visits (two) to determine eligibility (blood will be collected to measure IL-6, height and weight will be measured, a 4m walk test will be administered to determine gait speed, and a review of medical history, medications, a physical exam, and blood safety labs will be conducted to ensure safety to proceed/eligibility). Randomization to study drug or placebo will take place within 60 days of the first in-person screening visit and subsequent injections will take place every 4 weeks for 24 weeks. Participants will undergo physical function testing (400m walk, preferred & fixed speed walk on a treadmill with oxygen consumption measurement, short physical performance battery, grip strength, actigraphy), cognitive testing, and aortic pulse wave velocity and endothelial function testing. Height, weight and pulse will be measured. Participants will complete questionnaires to assess demographics, physical activity level, fatigability, sleep quality, pain and depression. Blood will be collected/processed to measure immune function and stored frozen to create a biorepository of samples (serum, plasma, buffy coat) for future testing. Participants will be monitored for safety in between injection visits and for 5 months following the final in-person research visit.

Conditions

Inflammation; Frailty

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Clazakizumab

Participants received Clazakizumab 5 mg as a subcutaneous injection every 4 weeks for 24 weeks

Group Type: EXPERIMENTAL

Clazakizumab

Intervention Type: DRUG

5 mg, subcutaneous injection, every 4 weeks for 24 weeks

Placebo

Participants received Clazakizumab placebo as a 5 mg subcutaneous injection every 4 weeks for 24 weeks

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

5 mg, subcutaneous injection, every 4 weeks for 24 weeks

Interventions

Clazakizumab

5 mg, subcutaneous injection, every 4 weeks for 24 weeks

Intervention Type: DRUG

Placebo

5 mg, subcutaneous injection, every 4 weeks for 24 weeks

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Persons aged ≥ 70 years at time of randomization
• Gait speed ≥ 0.44 m/sec to < 1.0 m/sec or BMI ≥ 28 kg/m2
• IL-6 level ≥ 2.0 pg/ml but < 30.0 pg/ml
• Self-reported difficulty walking ¼ mile or climbing 10 steps
• Self-reported ability to walk 400 meters (about 2-3 blocks), unassisted
• Self-reported vaccinations for COVID-19, Influenza and pneumococcal pneumonia up to date per current CDC guidelines

Exclusion Criteria

• Advanced neurologic disorder such as dementia, Parkinson's disease, amytrophic lateral sclerosis, or multiple sclerosis that would impact the ability to improve on functional assessments
• Resident in a nursing home
• Severe hearing or vision loss that would impair participant's ability to complete questionnaires or follow oral instructions, and which may limit feasibility of performing functional assessments
• Acute infections (including but not limited to common cold virus, shingles virus, bronchitis, skin infection, urinary tract infection, tooth abscess) within 60 days of randomization
• Chronic infection (including but not limited to):

• History of active TB or evidence of latent TB based on a positive PPD skin test, positive Quantiferon TB-Gold test, or a history of old or latent TB on chest x-ray
• History of Hepatitis B or Hepatitis C
• Previous diagnosis of Human Immunodeficiency Virus (HIV) or Acquired ImmunoDeficiency Syndrome (AIDS)
• Inflammatory or autoimmune disease (including but not limited to rheumatoid arthritis, lupus, or inflammatory bowel disease, such as ulcerative colitis or Crohn's disease)
• Immunization with a live/attenuated vaccine within 2 months prior to randomization (e.g., viral: measles vaccine, mumps vaccine, rubella vaccine, live attenuated influenza vaccine, live attenuated chicken pox or shingles vaccine, smallpox vaccine, oral polio vaccine (Sabin), rotavirus vaccine, and yellow fever vaccine. Bacterial: BCG vaccine, oral typhoid vaccine and epidemic typhus vaccine)
• Current use of chronic immune modulating medications such as corticosteroids, monoclonal antibodies, janus kinase inhibitors, calcineurin inhibitors, mTOR inhibitors, IMDH inhibitors, or biologics
• Admitted for an overnight hospitalization in the last 6 months
• Open-chest heart surgery (including, but not limited to, coronary artery bypass graft surgery or aortic valve surgery) in the past 6 months
• Anticipating major surgery (including, but not limited to, chest, abdomen, or joint surgery) in the next 6 months
• Deep vein thrombosis or pulmonary embolus in the past 6 months
• Severe lung disease or heart disease that requires oxygen use anytime during the day (including, but not limited to, use only during activity, use only at night or use all day)
• Tobacco use (including cigarettes, cigar, pipe, or vaping) or inhaled cannabis in the past 6 months
• Current consumption of > 14 alcoholic drinks per week
• History of substance abuse including cocaine, methamphetamine, opioids, or narcotics; any use of cannabis
• Uncontrolled diabetes, noncompliant with treatment or fasting glucose > 250 mg/dL
• Cancer: Stage 1 cancer (including melanoma skin cancers) within the past 5 years, other than adequately treated (fully excised and recovered from surgery based on the judgement of a study MD) basal and/or squamous cell skin cancer, or stage 2 or stage 3 cancer within 10 years, or any history of stage 4 (metastatic) cancer
• Inability to get a normal systolic blood pressure reading (between 100-180) at two consecutive visits prior to randomization (must be at least 1 day apart)
• ALT, AST, or Total Bilirubin > Upper Limit of Normal (ULN)
• Absolute Neutrophil Count outside normal range or < 1.5 x109/L
• White Blood Count outside normal range
• Platelet count outside normal range or < 125 x109/L
• Hemoglobin <10 g/dL
• Total Cholesterol > 300 mg/dL or Triglycerides > 400 mg/dL
• Dialysis treatment or chronic renal insufficiency defined as CKD-EPI eGFR < 25 ml/min/(1.73) m2
• History of diverticular disease or GI perforation
• History of severe allergic or anaphylactic reactions to human, humanized, or murine monoclonal antibodies
• Current use of Warfarin (Coumadin, Jantoven)
• Unable or unwilling to provide informed consent
• Current participation in another interventional study (including trials of exercise, diet, or investigational drugs)
• A psychiatric disorder that is impairing ability to consent or comply with requirements of the trial
• Residence or travel outside of the study area for more than one month during the study or planning to move out of the area in the next six months.
• Other conditions which at the discretion of a study physician investigator which would make participation unsafe or inappropriate (logistic, behavioral, medical)

• Minimum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

CSL Behring

INDUSTRY

Sponsor Role: collaborator

Anne B. Newman

OTHER

Sponsor Role: lead

Responsible Party

Anne B. Newman

Professor

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Anne B. Newman, MD, MPH

Role: PRINCIPAL_INVESTIGATOR

University of Pittsburgh

Locations

University of Pittsburgh, Health Studies Research Center

Pittsburgh, Pennsylvania, United States

Countries

United States

Other Identifiers

STUDY19030225

Identifier Type: -

Identifier Source: org_study_id