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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06159725
Other study ID # CMTX101-P1-CT002
Secondary ID
Status Recruiting
Phase Phase 1/Phase 2
First received
Last updated
Start date January 17, 2024
Est. completion date February 2025

Study information

Verified date February 2024
Source Clarametyx Biosciences, Inc.
Contact Teresa Byrne
Phone 4844677678
Email tbyrne@clarametyx.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

CMTX-101 is a bacterial biofilm disrupting monoclonal antibody being developed as an adjunctive therapy to standard of care antibiotics. The goal of this clinical trial is to assess the safety and tolerability of CMTX-101 in people with cystic fibrosis (pwCF). The main questions the study aims to answer are: - Are single doses of CMTX-101 IV infusion safe and tolerated - What is the pharmacokinetic (PK) profile of single doses of CMTX-101 - Do single doses of CMTX-101 induce development of anti-drug antibodies (ADA) and neutralizing antibodies (Nabs)


Recruitment information / eligibility

Status Recruiting
Enrollment 41
Est. completion date February 2025
Est. primary completion date February 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Adults =18 years of age at the time of screening. 2. Confirmed CF diagnosis based on current CF Foundation (CFF)-sponsored guidelines. 3. For participants on modulator therapy, they must be on a stable dose of TRIKAFTA (ETI) modulator therapy for at least 3 months. 4. Willing and capable of providing induced sputum for evaluation at defined study timepoints. 5. Positive P. aeruginosa growth of =104 CFU/gram from a sample of induced sputum at the screening visit. 6. FEV1 =50% (Part1) or =35% (Part 2) of predicted normal value at screening. 7. Currently receiving inhaled tobramycin alone or CAT therapy. At least one 28-day cycle completed within 8 weeks prior to screening visit. • Note: If on CAT therapy, initiation of inhaled tobramycin should begin approximately 2 hours (±1 hour) pre-dose. 8. Women of childbearing potential (WOCBP) must have a negative serum beta-human chorionic gonadotropin test during screening and agree to use an effective method of contraception for the duration of the study and for 4 months after the last infusion of study drug. A female participant is considered of childbearing potential unless postmenopausal or surgically sterilized and at least 3 months has passed since sterilization procedure. Female surgical sterilization procedures include tubal ligation, bilateral salpingectomy, hysterectomy, or bilateral oophorectomy. A female participant is considered postmenopausal if she has had spontaneous amenorrhea for at least 2 years with an appropriate clinical profile (e.g., age appropriate, history of vasomotor symptoms). • Effective methods of contraception include (a) abstinence, (b) partner vasectomy, (c) intrauterine devices, (d) hormonal implants (such as Implanon), or (e) other hormonal methods (birth control pills, injections, patches, vaginal rings). 9. Male participants with a female partner must use a medically accepted contraceptive regimen during his participation in the study and for 4 months after study drug infusion. • Acceptable methods of contraception for male participants include condoms with spermicide, surgical sterilization of the participant (i.e., vasectomy) at least 26 weeks before screening, or sexual abstinence (i.e., refraining from heterosexual intercourse) if that is the preferred and usual lifestyle of the participant. 10. Male participants must agree to abstain from sperm donation through 4 months after study drug administration. 11. Capable of providing informed consent. 12. Capable and willing to complete all study visits and perform all procedures required by the protocol. Exclusion Criteria: 1. Body mass index (BMI) <14 at screening and baseline. 2. Has a known history or evidence of human immunodeficiency virus (HIV) infection or chronic hepatitis B screening. 3. Tests positive for hepatitis C virus (HCV) RNA at screening. 4. Changes in underlying therapy (e.g., pulmonary massage therapy, bronchodilators, nonsteroidal anti-inflammatory drugs [NSAIDs], antibiotic agents, pancreatic enzyme preparations, nutritional supplements, and DNase) within the 21 days before, and inclusive of, study baseline or anticipated changes to underlying therapy during the study. 5. Pulmonary exacerbation within 28 days of baseline. 6. Requirement for continuous (24 hour/day) oxygen supplementation; periodic use is permitted. 7. Participation in smoking or vaping activity in the last 6 months. 8. History of, or planned, organ transplantation. 9. Elevated liver function tests obtained at screening. 1. ALT >5 × ULN or AST >5 × ULN, or 2. Total bilirubin >3 × ULN or Total bilirubin >1.5 × ULN combined with either ALT >3 × ULN or AST >3 × ULN. ULN reflects local laboratory ranges. 10. Greater than 5 ml of hemoptysis on one occasion or >30 mL of hemoptysis in a 24-hour period within 28 days of baseline. 11. Infection with other more pathogenic organisms such as Mycobacterium abscessus or Burkholderia spp., where the investigator feels that the participant either is not or will not remain clinically stable throughout the duration of the study. 12. Acute clinical illness requiring a new (oral, parenteral, or inhaled) antibiotic(s) =30 days prior to the baseline visit. Does not include chronic suppressive medications or cyclic dosing medications such as inhaled antibiotics. 13. Women who are pregnant, planning to become pregnant during the study period or for 4 months following last infusion of study drug, or breastfeeding. 14. Active treatment of any mycobacterial or fungal organisms =30 days prior to baseline visit. Chronic treatment for suppression of fungal populations is allowable. 15. Anticipated need to change chronic (either inhaled or oral) antibiotic regimens during the study period. Participants must agree to maintain their current chronic antibiotic regimen from the screening visit for the duration of the follow-up period (approximately 30 days). 16. Known allergy to any component of the study drug. 17. Participant with an estimated glomerular filtration rate <60 mL/min/1.73 m2. 18. Any significant finding that, in the opinion of the investigator, would make it unsafe for the participant to participate in this study or would not be in the best interest of the participant. 19. Enrolled in an interventional clinical study within =60 days of the baseline visit, or participating in a clinical study while enrolled in this clinical study (inclusive of vaccine studies). 20. Currently or previously enrolled in this study.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
CMTX-101
CMTX-101 is a humanized monoclonal antibody administered as a single IV infusion over approximately 60 minutes.
Placebo
Placebo is normal saline administered as a single IV infusion over approximately 60 minutes.

Locations

Country Name City State
United States University of Michigan Ann Arbor Michigan
United States St Luke's Sleep Medicine and Research Center Boise Idaho
United States Boston Children's Hospital Boston Massachusetts
United States Rainbow Babies and Children's Hospital/University Hospitals Cleveland Medical Center Cleveland Ohio
United States Nationwide Children's Hospital Columbus Ohio
United States National Jewish Health Denver Colorado
United States New York Medical College Hawthorne New York
United States PennState Health Hershey Pennsylvania
United States Central Florida Pulmonary Group, PA Orlando Florida
United States Stanford University Palo Alto California
United States University of Utah Salt Lake City Utah
United States Seattle Children's Hospital Seattle Washington

Sponsors (1)

Lead Sponsor Collaborator
Clarametyx Biosciences, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number and % of participants experiencing adverse events following a single IV infusion of CMTX-101 Primary objective Day 1 to Day 28
Primary Number and % of participants experiencing serious adverse events following a single IV infusion of CMTX-101 Primary objective Day 1 to Day 28
Secondary Assess the CMax - observed maximum plasma concentration determined by ELISA following a single IV infustion of CMTX-101 Secondary objective Day 1 to Day 35
Secondary Assess the TMax - time to reach maximum concentration curve following a single IV infusion of CMTX-101 Secondary objective Day 1 to Day 35
Secondary Assess the AUC0-8 Area under the concentration time curve from zero to infinite time following a single IV infusion of CMTX-101 Secondary objective Day 1 to Day 35
Secondary Assess the Terminal phase elimination rate determined by ELISA following a single IV infusion of CMTX-101 Secondary objective Day 1 to Day 35
Secondary Assess the Terminal elimination half- determined by ELISA following a single IV infusion of CMTX-101 Secondary objective Day 1 to Day 35
Secondary Assess the Apparent total body clearance (CL/F) determined by ELISA following a single IV infusion of CMTX-101 Secondary objective Day 1 to Day 35
Secondary Assess the Apparent volume distribution (Vx/F) determined by ELISA following a single IV infustion of CMTX-101 Secondary objective Day 1 to Day 35
Secondary Evaluate the immunogenicity of CMTX-101 as measured by anti-drug antibodies (ADA) determined by the electrochemiluminescence assay following a single IV infustion of CMTX-101 Secondary objective Day 1 to Day 35
Secondary Assess the apparent reduction in pulmonary P. auriginosa burden as measured by quantitative microbial culture of sputum Secondary objective Day 1 to Day 28
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