Proof of Principle Study for an Efficacy Trial of Linaclotide for Cystic Fibrosis

Trial statusRecruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
Age18-65
SponsorUniversity of Nottingham

About this trial

Linaclotide is a medicine used to treat constipation and irritable bowel syndrome with constipation (IBS-C). It works by acting on the surface of the gut lining, where it increases the movement of salt and water into the bowel. This softens stools, makes them easier to pass, and can also reduce gut pain

One advantage of linaclotide is that, unlike some natural substances in the gut, it is stable and can act throughout the intestine. Studies in animals show that it has the strongest effect in the upper small intestine, but it may act in other parts of the bowel as well. In people, however, it is not yet clear whether linaclotide mainly works in the small intestine or in the large intestine (colon). Knowing this is important, because it could help the investigators understand whether linaclotide might also be useful in other conditions, such as cystic fibrosis, where the gut does not handle fluid properly.

Linaclotide is taken as a capsule, but less than 1% is absorbed into the bloodstream. Instead, it stays in the gut, where it is broken down into smaller active parts. This means both the small intestine and colon may be exposed to its effects.

Until now, it has been hard to study this because traditional methods only measure one part of the gut at a time. A team at the University of Nottingham has developed MRI scanning methods that can safely and non-invasively measure water content in the small intestine and colon.

The aim of this pilot study is to use MRI in healthy volunteers to see exactly where linaclotide acts. This knowledge will help optimise future studies in conditions such as cystic fibrosis.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Crossover

Treatments tested in this trial

  • Linaclotide 290 micrograms

    Drug

    290 mcg, 2 days dosing, oral capsule form

  • Lactose placebo pill

    Drug

    Placebo form, oral capsules identical to linaclotide

Treatment groups

26 Participants
are divided into 2 treatment groups
Group A: LinaclotideExperimental treatment 1 intervention
Group B: PlaceboPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Small bowel water content

Area under curve (AUC) 0-360 minutes Water content in small bowel as assessed by MRI (mL)

Time frame
Baseline, and 0, 60, 120, 180, 240, 300, 360 minutes post-dose

Secondary outcomes

1

Colon water content

Area under curve (AUC) 0-360 min Water content in the ascending colonic region as assessed by MRI (mL)

Time frame
Baseline, and 0, 60, 120, 180, 240, 300, 360 minutes post-dose
2

Colonic regional segmental volumes

Total volume of regional colonic segments (ascending, transverse, descending, sigmorectal) as assessed by MRI (mL) at each time point.

Time frame
Baseline, and 0, 60, 120, 180, 240, 300, 360 minutes post-dose
3

Changes in stool consistency

Stool consistency rated using Bristol stool scale (type 1-7; 7 being watery stool).

Time frame
2 days before intervention, 5 days post-intervention
4

Changes in whole gut transit time (WGTT)

Assessed by time to stool discolouration following administration of blue dye paste.

Time frame
1 day post-intervention

Other outcomes

Sponsors and contacts

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