SPAN: A Phase 2, Open Label, Multicenter, Pilot Study to Assess Safety and Efficacy of an Enteric Microgranule Formulation of Adrulipase in Patients With Exocrine Pancreatic Insufficiency (EPI) Due to Cystic Fibrosis (CF)

Status: Completed
Location: See all (3) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Some cystic fibrosis patients are unable to digest food and absorb nutrition appropriately as they have a condition known as exocrine pancreatic insufficiency (EPI). Currently, these patients take pancreatic enzymes that are obtained from pig pancreas to aid the digestion of food. The goals of this clinical study are to evaluate the safety and efficacy of a novel formulation of a non-porcine lipase, called adrulipase, in patients with EPI due to cystic fibrosis. The main question\[s\] the study aims to answer are: 1. Is the novel formulation of adrulipase safe to use at the doses being evaluated in the clinical study. 2. Is adrulipase as effective, or more effective, compared to the pig enzymes the patients currently use. Researchers will compare the results obtained with adrulipase to how the patients typically respond to their pig enzymes to see if adrulipase helps patients digest fats adequately and if their stomach feels good (signs and symptoms of malabsorption).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• A confirmed diagnosis of cystic fibrosis, based on 2 clinical features consistent with CF, plus either a new/historic sweat chloride \>60 mmol/L by quantitative pilocarpine iontophoresis (measured while not on a CFTR modulator) or genotype.

• On stable dose of porcine PERT ≥1 month (30 days) prior to screening; stable dose is defined as dose of medication not changed during this time period, and the medication must be commercially available and be administered in the recommended dose range.

• CFA = or \> 80% at screening while on stable PERT

• A fair or better nutritional status as defined by:

‣ BMI ≥16.0 kg/m2 for female patients ≥18 years of age, or

⁃ BMI ≥16.5 kg/m2 for male patients ≥18 years of age

• Fecal elastase \<100 µg/g of stool at screening

• Standard-of-Care medications including CFTR modulators are allowed

Locations
United States
Florida
Central Florida Pulmonary Group
Orlando
Illinois
The Cystic Fibrosis Institute
Northfield
Nevada
Childrens Lung Specialists
Las Vegas
Time Frame
Start Date: 2023-02-01
Completion Date: 2023-07-28
Participants
Target number of participants: 13
Treatments
Experimental: Adrulipase
Upon study enrolment, the patient will be switched from their commercial PERT to receive adrulipase. Patients will initially receive a low dose of adrulipase. Upon the appearance of EPI symptoms, lasting at least three days, and upon discussion with the investigator, the patient will be switched to the medium dose of adrulipase. If signs and symptoms of EPI persist for three or more days, the patient will be switched to the high dose of adrulipase.
Sponsors
Leads: Entero Therapeutics

This content was sourced from clinicaltrials.gov