Overview

Double-blind, randomised, placebo-controlled phase II / III trial evaluating efficacy and safety of two different doses (2 g/d or 3 g/d) of oral controlled-ileocolonic-release nicotinamide (CICR-NAM) compared to placebo in patients with ulcerative colitis (UC).

The intended therapeutic use of CICR-NAM is to improve intestinal inflammation in adults with UC by topically increasing nicotinamide supply in the ileocolonic region and thus favourably influencing the composition of intestinal microbiota

Eligibility

Inclusion Criteria:

General

1. Male and female patients with UC and 18 to 80 years of age (at the time of signing the informed consent).
2. Ability to understand and comply with the protocol.
3. Signed written informed consent.

   Disease-specific:

4. Documented diagnosis of UC, with a minimum disease duration of 3 months prior to screening and ≥ 1 relapse, clinically defined using established criteria within the last 12 months.
5. Histology supportive for the diagnosis of UC.
6. Mild to moderate disease activity (at screening): modified Mayo score (mMS) 4-7 RB ≥ 1, endoscopic score ES ≥1 and SF ≥ 1.
7. RHI > 4 (at screening endoscopy).
8. Disease extent >15 cm from the anal verge (at screening endoscopy).
9. Elevated level(s) of C-reactive protein (CRP) and/or faecal calprotectin during the screening period (levels above the reference range, measured by local laboratories).
10. Full colonoscopy with no signs of malignancy either during screening or within one year before screening.

    Medication

11. In the case of no oral 5-aminosalicylate (5-ASA) therapy within the last 2 weeks

    before entry into screening with informed consent, any prior oral 5-ASA therapy is permitted and the patient is not allowed to receive 5-ASA during the study. In the case of oral 5-ASA therapy within 2 weeks before entry into screening with informed consent, the 5-ASA therapy should have been ongoing for > 3 months and should be stable ≥ 4 weeks before screening endoscopy with ≤ 3 g/d (up to 3 days with > 3 g/d acceptable). This 5-ASA baseline medication must be kept stable in the induction period and may be reduced (but not increased again) in the maintenance period.

Exclusion Criteria:

General health and UC:

1. Diagnosis of CD, microscopic colitis, ischaemic colitis, radiation colitis or indeterminate colitis.
2. Infectious colitis, diverticulitis or segmental colitis associated with diverticulosis (SCAD) within the last 6 months before screening.
3. Current or past diagnosis of complex fistulae, intra-abdominal or peritoneal abscesses, strictures with obstructive symptoms.
4. Severe UC disease activity (modified Mayo score >7).
5. Severe extraintestinal manifestations of UC requiring special treatment.
6. Steroid-dependent or steroid-refractory UC.
7. Foreseeable need for hospitalisation.
8. Previous colonic surgery, except for appendectomy.
9. Stools positive for enteric pathogens; Clostridium difficile toxin (CDT)-positive infection; indications for other relevant infections including cytomegalovirus colitis, each at screening.
10. Current or history of colon carcinoma, high grade colonic dysplasia or other malignancies except for completely resected basal cell carcinoma and squamous cell carcinoma of the skin.
11. Moderate to severe anaemia (haemoglobin <9 g/dL) at screening.
12. Moderate to severe renal impairment (glomerular filtration rate <60) at screening.
13. Relevant bleeding or thrombotic disorders.
14. Alcohol or drug abuse within the last 2 years.

    Medications

15. Rectal topical 5-ASA and/or rectal budesonide therapy (enemas, foams or

    suppositories) ≤ 2 weeks prior to screening endoscopy (up to 3 single doses allowed).

16. Use of oral corticosteroids and/or oral budesonide ≤ 4 weeks prior to screening endoscopy.
17. Previous use of immunosuppressants, Janus kinase inhibitors, sphingoside-1-phosphate receptor modulators or biologics.
18. Use of antibiotics for the treatment of UC or probiotic medication within 6 weeks prior to screening endoscopy.
19. Any need of parenteral therapies for the therapy of UC (except iron infusions).
20. Known hypersensitivity towards any component of the CICR-NAM or placebo tablets.

    Regulatory requirements

21. Participation in a clinical trial within 4 weeks prior to screening for this trial or intake of an investigational medicinal product (IMP) within the last 8 weeks or 5 half-lives (whichever is longer) prior to screening (or longer if necessary in the investigator's discretion).
22. Patients under legal supervision or guardianship, including patients, who are committed to an institution by virtue of an order issued either by the judicial or the administrative authorities.
23. Patients who are dependent on the investigator or the sponsor.

    Other

24. Pregnant or breastfeeding women.
25. Women of childbearing potential (WoCBP) not using highly effective contraception till at least 1 month after last dosing of IMP.
26. Male participants with female partners of childbearing potential who are not willing to use a highly effective contraception till at least 1 month after last dosing of IMP.
27. Indications that the patient may be unable to comply with the trial procedures, e.g. language barriers precluding adequate understanding or cooperation.
28. Any circumstances or medical conditions which could contradict a trial participation and lead the investigator to assess the patient as unsuitable for trial participation for any other reason.