ANG003 for Cystic Fibrosis
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores a new treatment called ANG003, an experimental therapy, for individuals with cystic fibrosis who struggle with digestion due to exocrine pancreatic insufficiency (EPI). The goal is to determine if ANG003 is safe and as effective as Creon, a currently approved enzyme therapy. Participants will try different doses of ANG003 or continue using Creon to assess which is more effective. Those with cystic fibrosis who regularly use enzyme replacement therapy and have a controlled form of EPI might be suitable candidates. As a Phase 2 trial, this research focuses on evaluating the treatment's effectiveness in an initial, smaller group, offering participants a chance to contribute to significant advancements in cystic fibrosis care.
Do I have to stop taking my current medications for the trial?
The trial does not specify if you need to stop taking your current medications, but it requires that you have been on a stable dose of pancreatic enzyme replacement therapy for 90 days before the screening.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that ANG003 has been tested for safety in people with cystic fibrosis. In earlier studies, most participants tolerated ANG003 well, experiencing only mild side effects that were not serious. ANG003 functions similarly to other enzyme treatments for pancreatic issues, such as Creon, suggesting it should be safe. However, further research is needed to confirm this. Previous studies indicate it might be a helpful option for those needing enzyme replacement therapy.12345
Why do researchers think this study treatment might be promising?
Researchers are excited about ANG003 for cystic fibrosis because it offers a potentially new approach to managing the condition. While standard treatments like Creon focus on enzyme replacement to aid digestion, ANG003 is being tested to see if it can improve digestion differently, possibly offering a more effective or faster-acting solution. The trial is exploring different doses of ANG003, which might help tailor the treatment to individual needs, potentially enhancing its effectiveness. If successful, ANG003 could provide a significant advancement in the quality of life for those with cystic fibrosis.
What evidence suggests that ANG003 could be an effective treatment for exocrine pancreatic insufficiency in cystic fibrosis?
Research has shown that ANG003, a non-pig enzyme treatment, may improve fat absorption in people with cystic fibrosis. This trial will test different doses of ANG003, including Dose A and Dose B, to evaluate their effectiveness. Studies indicate that ANG003 significantly enhances the absorption of essential fatty acids like DHA and EPA, which are crucial for good health. Evidence suggests that ANG003 might be effective at lower doses than other enzyme treatments derived from pigs. This could make it a strong option for those with exocrine pancreatic insufficiency, as it aids in the digestion and absorption of nutrients.12567
Are You a Good Fit for This Trial?
This trial is for people aged 12 and older (in the US) or 18 and older (in the EU) who have cystic fibrosis with severe pancreatic insufficiency. Participants must have a stable weight, be on a steady dose of enzyme therapy for at least 90 days, and meet certain BMI requirements.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Acclimation
All subjects will be acclimated to Creon for 14 days and undergo a baseline CFA analysis
Treatment
Participants are randomized to ANG003 Dose A, ANG003 Dose B, Creon, or Off Enzyme for 21 days with subsequent CFA analysis
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- ANG003
Trial Overview
The study compares two doses of ANG003, a new enzyme replacement therapy, to Creon (an approved enzyme treatment), to see if ANG003 is safe and works as well as Creon in treating pancreatic insufficiency caused by cystic fibrosis.
How Is the Trial Designed?
5
Treatment groups
Experimental Treatment
Active Control
All subjects will be acclimated to Creon for 14-days and then will undergo a baseline CFA analysis. If baseline CFA is \>/= 80%, the subject may be randomized to ANG003 Dose B for a 21-day acclimation and subsequent CFA analysis.
All subjects will be acclimated to Creon for 14-days and then will undergo a baseline CFA analysis. If baseline CFA is \>/= 80%, the subject may be randomized to ANG003 Dose A for a 21-day acclimation and subsequent CFA analysis.
All subjects will be acclimated to Creon for 14-days and then will undergo a baseline CFA analysis. Participants with a Period A CFA result of 60% to \<80% will be assigned to ANG003 Dose B.
All subjects will be acclimated to Creon for 14-days and then will undergo a baseline CFA analysis. If baseline CFA is \>/= 80%, the subject may be randomized to Creon for an additional 21-days and subsequent CFA analysis.
All subjects will be acclimated to Creon for 14-days and then will undergo a baseline CFA analysis. If baseline CFA is \>/= 80%, the subject may be randomized to the off enzyme arm. Subjects will receive Creon for an additional 21-day and the subsequent CFA analysis will be off enzyme. Total time off enzyme will be 4-7 days.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Anagram Therapeutics, Inc.
Lead Sponsor
Citations
Results of a clinical trial of ANG003, a non-porcine ...
Results for ANG003 protease and amylase activity suggest that doses lower than those in current porcine-derived PERTs may be efficacious.
Phase 2 Study to Assess the Safety and Efficacy of ANG003
In this study, ANG003, a pancreatic enzyme replacement therapy (PERT; commonly called "enzymes"), is being investigated as a potential treatment for ...
Results of a clinical trial of ANG003, a non-porcine ...
ANG003 lipase significantly improves DHA+EPA and total fat absorption in a dose dependent manner. Results for ANG003 ... cystic fibrosis (CF). We ...
ANG003 is a Novel Non-Porcine Enzyme Replacement for ...
“Data reported on ANG003 at the North American Cystic Fibrosis Conference exceeded our expectations, exhibiting a robust increase in DHA and ...
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apps.cff.org
apps.cff.org/Trials/Finder?search=%7BPipelineDrugId%3A%2710209%27%2CPipelineDrugDisplayName%3A%27ANG003%27%7DClinical Trials Finder | CFF Clinical Trials Tool
This study will assess the safety and effectiveness of ANG003, a pancreatic enzyme replacement therapy, also known as “enzymes” or “enzyme therapy”, ...
Phase 1 Study to Assess Safety and Efficacy of ANG003
Also called a data safety and monitoring board ... Safety and Efficacy of ANG003 in Patients With Exocrine Pancreatic Insufficiency Due to Cystic Fibrosis.
Anagram Therapeutics Completes Dosing Study of ...
The primary objective of this multicenter, randomized, parallel study was to evaluate the safety and dose ranging of orally administered ANG003 ...
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