CLINICAL TRIAL / NCT05104853
Study to Evaluate the Safety, Tolerability, PDs, and Efficacy of CNP-104 in Subjects with Primary Biliary Cholangitis
- Interventional
- Recruiting
- NCT05104853
A Phase 2a Double Blind, Placebo Controlled Study to Evaluate the Safety, Tolerability, Pharmacodynamics, and Efficacy of CNP-104 in Subjects Ages 18-75 with Primary Biliary Cholangitis Who Are Unresponsive to UDCA And/or OCA
This study is a Phase 2a First-in-Human (FIH) clinical trial to assess the safety, tolerability, pharmacodynamics (PD), and efficacy of multiple ascending doses of CNP-104. The study consists of a 120 day primary study followed by a 20 month long-term safety and durability of response follow-up period.
Subjects ages 18-75 with primary biliary cholangitis will be screened up to 14 days prior
to enrollment into the study. Screening will be completed to assess eligibility, obtain
vital signs, collect laboratory samples and PD measurements, and to receive a FibroScan
for liver fibrosis. Subjects will additionally complete an initial PBC-40 assessment and
begin an Itch Diary, a questionnaire and scoring system to be completed by the patient
every morning and evening through Day 120 and then monthly through end of study.
Subjects who meet all inclusion and no exclusion criteria after completing the screening
visit will be enrolled in the study. Subjects will be randomized on Day 1 in a 1:1 ratio
to receive either CNP-104 or Placebo (0.9% Sodium Chloride USP) by intravenous (IV)
infusion. Subjects will be administered CNP-104 or Placebo on Day 1 and on Day 8. This
study was originally designed with 2 cohorts, Cohort 1 comprised of 6 subjects randomized
1:1 to placebo or 4 mg/kg, and Cohort 2 comprised of up to 34 subjects randomized 1:1 to
placebo or 8 mg/kg. Under Protocol Amendment 6 (v7.0), the remaining subjects for Cohort
2 (approximately 16) will be randomized 1:3:1 to placebo, 4 mg/kg, and 8 mg/kg
respectively.
Subjects will remain in the clinic on Day 1 and Day 8 from the time of admission (prior
to administration of CNP-104 or Placebo) through the final procedure conducted 4 hours
post-dose that same day unless an infusion reaction, or other adverse event, requires an
extended duration of monitoring. Subjects will be discharged if safety parameters are
acceptable to the investigator.
Seven days after the second administration of CNP-104 or Placebo, subjects must return to
the clinic for collection of safety labs, PD measurements, and assessment of AEs and
medication changes.
Subjects will continue to be followed for 2 years to assess safety, pharmacodynamics, and
immunogenicity during the Post-Dosing period.
Gender
All
Age Group
18 Years to 75 Years
Accepting Healthy Volunteers
No
Inclusion Criteria:
1. Subjects who are willing and able to provide Institutional Review Board (IRB)
approved written informed consent and privacy language as per national regulations.
2. Men and non-pregnant women, ages 18-75 years inclusive.
3. Subjects with a PBC diagnosis as demonstrated by the presence of 2 or more of the
following 3 diagnostic factors:
1. Alkaline phosphatase > 1.5× ULN for at least 6 months
2. Positive AMA titer or, if AMA negative or in low titer (<1:40), positive
PBC-specific antibodies (anti-GP210 and/or anti-SP100 and/or antibodies against
the major M2 components [PDC-E2, 2-oxo-glutaric acid dehydrogenase complex])
3. Liver biopsy findings consistent with PBC
4. Subjects who are unresponsive to UDCA and/or OCA after 6 months of treatment at a
stable dose as measured by ALP > 1.5× ULN.
5. For subjects on any medication used to treat the symptoms of PBC (ex. UDCA, OCA,
seladelpar), subjects must be on a stable dose for a minimum of 3 months prior to
enrollment and must agree not to change their dose through study Day 60 unless
reviewed by the medical monitor and approved by the site investigator.
6. Subjects with ALP > 1.5× ULN.
7. Subjects with AST and ALT < 5× ULN.
8. Subjects with hemoglobin ≥ 10 g/dL.
9. Subjects with total bilirubin < 2× ULN.
10. Men and women of child-bearing potential (WOCBP) must agree to practice a highly
effective method of contraception that may include, but is not limited to,
abstinence, sex only with persons of the same sex, monogamous relationship with
vasectomized partner, vasectomy, hysterectomy, bilateral tubal ligation, licensed
hormonal methods, intrauterine device (IUD) beginning at the time of screening
through Day 90.
11. Female subjects who agree not to donate ova starting at initial screening and
through Day 90.
12. Male subjects who agree to not donate sperm starting at screening and through Day
90.
Exclusion Criteria:
1. Subjects with a Class B or Class C Child-Pugh score.
2. Subjects with concomitant liver diseases including chronic viral hepatitis B or C,
autoimmune hepatitis, PSC, alcoholic liver disease, Wilson's disease,
hemochromatosis, or Gilbert's syndrome.
3. Subjects who have previously undergone liver transplantation.
4. Subjects with decompensated liver disease as defined by the presence or history of
any of the following:
- MELD score > 15
- Hepatic encephalopathy
- Ascites
- Hepatorenal syndrome or serum creatinine > 2 mg/dL
- Total Bilirubin > 3.0 mg/dL
- INR >1.8 unless on anticoagulation such as Coumadin
- History of variceal hemorrhage
5. Subjects with a history of cerebrovascular accident in the past 12 months.
6. Subjects with history of myocardial infarction, as defined by any of the following
criteria:
- Development of pathological Q waves with or without symptoms
- Imaging evidence of a region of loss of viable myocardium that is thinned and
fails to contract, in the absence of a non-ischemic cause
- Pathological findings of a healed or healing myocardial
7. Subjects with chronic kidney disease, as defined by estimated glomerular filtration
rate (eGFR) < 60 mL/min/1.73 m2 for at least 3 months (per CKD EPI Equation - 2021).
8. Subjects with uncontrolled diabetes, as defined by HbA1c > 7%.
9. Subjects who have used the following medications:
- Methotrexate within 90 days of screening.
- Immunotherapy drugs unless approved by the medical monitor.
10. Subjects with a history of tuberculosis or positive PPD skin test.
11. Subjects who have received administration of any live vaccine (other than intranasal
Influenza) within 28 days or subunit vaccine within 14 days prior to screening or
are planning to receive any vaccination before Day 90.
12. Subjects who have used systemic steroids within 3 months prior to screening.
13. Subjects with laboratory test results at screening or prior to study dosing that are
outside the normal limits and considered by the Investigator to be clinically
significant.
Note: This criterion does not apply to liver function tests. Additionally,
clinically significant laboratory test results at screening that are related to the
condition (PBC) are acceptable as long as all inclusion and no other exclusion
criteria are met.
14. Subjects with positive test results for hepatitis B surface antigen (HBsAg),
hepatitis C virus (HCV) antibody, or human immunodeficiency virus (HIV)
antigen/antibody as determined at screening.
15. Subjects with a history of or currently active immune disorders other that PBC
(including autoimmune disease) unless the condition, after discussion with the
Medical Monitor, has been deemed to be acceptable for the subject's participation in
this study.
16. Subjects with a history of or current active diseases requiring immunosuppressive
drugs (including azathioprine, prednisone, prednisolone, budesonide, cyclosporine,
tacrolimus, methotrexate, or mycophenolate mofetil) unless the condition, after
discussion with the Medical Monitor, has been deemed to be acceptable for the
subject's participation in this study.
17. Subjects with a clinical history of significant cardiovascular disease as determined
by the Investigator.
18. Subjects with a complication or medical history of malignancy within past 5 years
which, in the Investigator's opinion, makes the subject unsuitable for study
participation.
19. Subjects who, in the Investigator's opinion, will be unable to adhere to study
procedures.
20. Subjects who have received an investigational therapy other than CNP-104 within 28
days or 5 half-lives, whichever is longer, prior to screening.
21. Subjects with any condition which, in the Investigator's opinion, makes the subject
unsuitable for study participation.
22. Known sensitivity to any components of CNP-104.