ClinicalTrials.gg
CompletedNCT06159725Updated Oct 30, 2026

A Study To Evaluate The Safety Of CMTX-101 In People With Cystic Fibrosis

A Phase 1/2 interventional study of CMTX-101 and Placebo in Persistent Infection and Cystic Fibrosis, sponsored by Clarametyx Biosciences, Inc.. Completed at 23 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-30.

Sponsored by Clarametyx Biosciences, Inc. · Phase 1/2, Interventional, and Treatment

Phase
Phase 1/2
Study type
Interventional
Enrollment
43
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study 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)
02

Conditions studied

  • Persistent Infection
  • Cystic Fibrosis

Keywords

  • Pseudamonas auriginosa
03

In context

Persistent Infection

44 studies on the registry are indexed under Persistent Infection; 5 are open to participants now.

This study's enrollment of 43 is below the median of 104 across 28 interventional studies indexed under Persistent Infection.

Browse Persistent Infection studies →

Lead sponsor

Clarametyx Biosciences, Inc. is the lead sponsor of 2 studies on the registry; none are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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. Adults ≥18 years of age at the time of screening.
  2. If enrolled in the CFF Patient Registry, must provide registry information.
  3. Confirmed CF diagnosis based on current CF Foundation (CFF)-sponsored guidelines.
  4. For participants on modulator therapy, they must be on a stable dose of modulator therapy for at least 3 months.
  5. Willing and capable of providing induced sputum for evaluation at defined study timepoints.
  6. Positive P. aeruginosa growth of ≥104 CFU/gram from a sample of induced sputum at the screening visit.
  7. ≥50% (Part1) or ≥35% (Part 2) of predicted normal value at screening.
  8. Currently receiving inhaled antibiotic therapy, either tobramycin or aztreonam alone, or as part of CAT. At least one 28-day cycle completed within 8 weeks prior to screening visit.
  9. Women of (WOCBP) must have a negative serum beta-human chorionic gonadotropin test during screening and agree to use an effective method of 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 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).
  10. 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.

    - Males with infertility documentation are not required to use contraception.

  11. Male participants must agree to abstain from sperm donation through 4 months after study drug administration.
  12. Capable of providing .
  13. Capable and willing to complete all study visits and perform all procedures required by the protocol.

Exclusion criteria

Exclusion Criteria:

  1. (BMI) \<14 at screening and baseline.
  2. Has a known history or evidence of (HIV) infection or chronic screening.
  3. Tests positive for virus (HCV) RNA at screening.
  4. Pulmonary exacerbation within 28 days of baseline.
  5. Requirement for continuous (24 hour/day) oxygen supplementation; periodic use is permitted.
  6. Participation in smoking or vaping activity in the last 6 months.
  7. History of, or planned, organ transplantation.
  8. Elevated liver function tests obtained at screening.

    1. >5 × or AST >5 × ULN, or
    2. Total >3 × ULN or Total bilirubin >1.5 × ULN combined with either ALT >3 × ULN or AST >3 × ULN. ULN reflects local laboratory ranges.
  9. Greater than 5 ml of hemoptysis on one occasion or >30 mL of hemoptysis in a 24-hour period within 28 days of baseline.
  10. 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.
  11. 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.
  12. Women who are pregnant, planning to become pregnant during the study period or for 4 months following last infusion of study drug, or breastfeeding.
  13. Active treatment of any mycobacterial or fungal organisms ≤30 days prior to baseline visit. Chronic treatment for suppression of fungal populations is allowable.
  14. 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).
  15. Known allergy to any component of the study drug.
  16. Participant with an estimated \<60 mL/min/1.73 m2.
  17. 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.
  18. 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).
  19. Currently or previously enrolled in this study.
Terms in these criteria, in plain language(13)

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.

FEV1

From a breathing test (spirometry): how much air you can blow out in the first second. Often given as a percentage of what is expected for your age, height and sex.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

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.

Postmenopausal

Periods have stopped for good: usually no period for 12 months in a row without another medical reason, sometimes confirmed by a blood test (FSH).

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

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.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
43 participants (actual)

Study arms

  • Placebo comparator
    Placebo

    Matching placebo, 100mL normal saline

    Drug: Placebo

  • Experimental
    5 mg/kg CMTX-101

    5mg/kg CMTX-101 in 100mL normal saline

    Drug: CMTX-101

  • Experimental
    30 mg/kg CMTX-101

    30 mg/kg CMTX-101 in 100mL normal saline

    Drug: CMTX-101

  • Experimental
    15 mg/kg CMTX-101

    15 mg/kg CMTX-101 in 100mL normal saline

    Drug: CMTX-101

Interventions

  • DrugCMTX-101

    CMTX-101 is a humanized monoclonal antibody administered as a single IV infusion over approximately 60 minutes.

  • DrugPlacebo

    Placebo is normal saline administered as a single IV infusion over approximately 60 minutes.

06

What researchers measure

Primary outcomes

  1. Number and % of participants experiencing adverse events following a single IV infusion of CMTX-101

    Primary objective

    Time frame: Day 1 to Day 28

  2. Number and % of participants experiencing serious adverse events following a single IV infusion of CMTX-101

    Primary objective

    Time frame: Day 1 to Day 28

Secondary outcomes

  1. Assess the CMax - observed maximum plasma concentration determined by ELISA following a single IV infustion of CMTX-101

    Secondary objective

    Time frame: Day 1 to Day 35

  2. Assess the TMax - time to reach maximum concentration curve following a single IV infusion of CMTX-101

    Secondary objective

    Time frame: Day 1 to Day 35

  3. Assess the AUC0-∞ Area under the concentration time curve from zero to infinite time following a single IV infusion of CMTX-101

    Secondary objective

    Time frame: Day 1 to Day 35

  4. Assess the Terminal phase elimination rate determined by ELISA following a single IV infusion of CMTX-101

    Secondary objective

    Time frame: Day 1 to Day 35

  5. Assess the Terminal elimination half- determined by ELISA following a single IV infusion of CMTX-101

    Secondary objective

    Time frame: Day 1 to Day 35

  6. Assess the Apparent total body clearance (CL/F) determined by ELISA following a single IV infusion of CMTX-101

    Secondary objective

    Time frame: Day 1 to Day 35

  7. Assess the Apparent volume distribution (Vx/F) determined by ELISA following a single IV infustion of CMTX-101

    Secondary objective

    Time frame: Day 1 to Day 35

  8. 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

    Time frame: Day 1 to Day 35

  9. Assess the apparent reduction in pulmonary P. auriginosa burden as measured by quantitative microbial culture of sputum

    Secondary objective

    Time frame: Day 1 to Day 28

07

Study locations

23 sites
  • University of Alabama, Birmingham
    Birmingham, Alabama 35294, United States
  • Stanford University
    Palo Alto, California 94304, United States
  • University of California, San Francisco
    San Franciso, California 94143, United States
  • National Jewish Health
    Denver, Colorado 80206, United States
  • Central Florida Pulmonary Group, PA
    Orlando, Florida 32803, United States
  • St Luke's Sleep Medicine and Research Center
    Boise, Idaho 83702, United States
  • Cystic Fibrosis Institute
    Northfield, Illinois 60093, United States
  • University of Kansas
    Kansas City, Kansas 66160, United States
  • Johns Hopkins University
    Baltimore, Maryland 21287, United States
  • Boston Children's Hospital
    Boston, Massachusetts 02115, United States
  • University of Michigan
    Ann Arbor, Michigan 48109, United States
  • New York Medical College
    Hawthorne, New York 10532, United States
  • Lenox Hill Hospital
    New York, New York 10075, United States
  • Rainbow Babies and Children's Hospital/University Hospitals Cleveland Medical Center
    Cleveland, Ohio 44106, United States
  • Nationwide Children's Hospital
    Columbus, Ohio 43205, United States
  • PennState Health
    Hershey, Pennsylvania 17003, United States
  • University of Pennsylvania
    Philadelphia, Pennsylvania 19104, United States
  • UPMC Children's Hospital of Pittsburgh
    Pittsburgh, Pennsylvania 15224, United States
  • Medical University of South Carolina
    Charleston, South Carolina 29425, United States
  • Vanderbilt University
    Nashville, Tennessee 37235, United States
  • University of Utah
    Salt Lake City, Utah 84132, United States
  • Virginia Commonwealth University
    Richmond, Virginia 23219, United States
  • Seattle Children's Hospital
    Seattle, Washington 98105, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Minor edits
Nothing that changes what the study is or who can join. Edited: verification date and registry dates
1 update, last Oct 30, 2026
Show all 1 update
  1. Oct 30, 2026
    Minor edits only
    + 2 other changes: verification date and registry dates

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT06159725
Lead sponsor
Clarametyx Biosciences, Inc.
Responsible party
Sponsor
First posted
Dec 7, 2023
Start date
Jun 24, 2024
Primary completion
Nov 14, 2025
Completion
Nov 14, 2025
Last update
Oct 30, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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