Effect of Bitopertin on the Liver and on Levels of Protoporphyrin IX in Bile, Blood, Liver, and Stool in Patients With Erythropoietic Protoporphyria/X-linked Protoporphyria and Increased Liver Stiffness and/or Liver Enzymes at Baseline

Wake Forest University (WFU)

Status and phase

Begins enrollment this month

Phase 1

Conditions

Protoporphyria

Treatments

Drug: bitopertin

Study type

Interventional

Funder types

Other

Identifiers

NCT07123363

IRB00118441

Details and patient eligibility

About

The primary goal of this study is to assess safety and tolerability of bitopertin in subjects with Erythropoietic Protoporphyria (EPP) or X-linked Protoporphyria (XLP) and evidence of compensated liver disease.

Full description

This in an open-label, investigator-initiated study of bitopertin (60 mg/day) in selected and carefully monitored participants with Erythropoietic Protoporphyria (EPP) or X-linked Protoporphyria (XLP) who have increased liver stiffness and/or elevated liver enzymes at baseline.This study is designed to evaluate whether bitopertin is effective in reducing hepatic and biliary levels of protoporphyrin IX (PP), which over time, with chronic and ongoing bitopertin treatment, will ameliorate and forestall progression of PP hepatopathy, providing an additional major benefit and reason for its chronic use in patients with EPP/XLP.

Enrollment

10 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Diagnosis of EEP or XLP that has been biochemically and genetically verified prior diagnosis of EPP or XLP
Age 18-75 years
Increased liver stiffness at baseline, defined as stiffness measurement [E value] by: Fibroscan >7 kPa; MRE that is >3.0 kPa; Velacur/Sonicincyte that is >6.0 kPa; and/or elevated liver enzymes: serum ALT > 2 X upper limit of normal (ULN), but not greater than 5 X ULN and/or serum AP > 2 X ULN, but not greater than 5 X ULN
INR < 1.4
Compensated liver disease at baseline, defined as lack of clinically evident ascites, encephalopathy, hepatocellular carcinoma, clinically evident icterus or jaundice, peripheral edema.
Willingness and ability to volunteer and provide informed consent for a long-term study that will include liver biopsies and collection of bile from the second portion of the duodenum, at baseline and at the end of study. In addition, follow-up visits will be planned every 26 weeks throughout the study, with plans for repeat routine/safety labs at each visit and for measures of liver stiffness and markers of hepatic status and fibrosis (Fib-4, APRI, ELF, Fibrotest) performed once every 6 months.

Exclusion criteria

Chronic hepatitis B, C, D, or E;
Human immunodeficiency (HIV) infection;
Alcohol use > 14 units/week for men or > 7 units/week for women;
Pregnancy or breast feeding among women;
Any known active malignancy other than small and localized squamous or basal cell carcinoma of the skin;
Advanced or decompensated heart, lung, kidney, liver, or neuro-psychiatric disease;
History of diagnosed depression or suicidality;
History of diagnosed substance abuse or poor impulse control;
Any other conditions that, in the opinion of the Investigator, renders the individual unfit to participate