Safety, Tolerability, Efficacy Study of PUR 0110 Rectal Enema in Mild-to-Moderate Distal Ulcerative Colitis

NCT ID: NCT01149707

Last Updated: 2018-05-01

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 34 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-06-01
• Study Completion Date: 2015-06-20

Brief Summary

PUR 0110 is a 100% natural novel investigational medicinal product that has been demonstrated in several in vitro and in vivo pharmacology studies to have potent anti-inflammatory, anti-oxidative and immunomodulatory effects. This exploratory Phase 2a study is a first-in-patient study to evaluate the safety, tolerability, biomarker effect and efficacy of PUR 0110 rectal enema in patients with active mild-to-moderate distal ulcerative colitis (UC).

The study is a multicenter, randomized, double-blind, parallel-group, dose-ranging, placebo-controlled study. To be eligible for inclusion into the study, patients must either be newly diagnosed or have on-going active mild-to-moderate distal ulcerative colitis of at least 3 months duration confirmed in either case by flexible sigmoidoscopy and biopsy at the Screening Visit. In addition, patients must have a modified Mayo score of ≥5 to ≤10 including a sigmoidoscopy inflammation grade and rectal bleeding scores of ≥2 each. Eligible patients will be randomly assigned to receive either PUR 0110 250 mg, 500 mg or 1000 mg or placebo rectal enema in a 1:1:1:1 ratio. Patients will self-administer the assigned study medication intrarectally once-daily at bedtime (10:00 p.m +/- 1 hour) for 2 weeks.

Patients will be evaluated for safety by adverse events, clinical laboratory tests, vital signs, physical examination, electrocardiogram (ECG), and concomitant medications. Efficacy evaluations will include the modified Mayo score, patient-defined response and remission, Investigator Assessment of Ulcerative Colitis Symptom Score, Inflammatory Bowel Disease Questionnaire (IBDQ), and biomarkers of inflammation, apoptosis and total cell death, lipid peroxidation and in vivo oxidative stress, and antioxidant defense mechanisms in plasma, serum, urine, feces and biopsy tissue. Patients will have a flexible sigmoidoscopy and biopsy 12 hours after the last dose of study medication.

Detailed Description

Safety/Primary Outcome Parameters:

• Incidence, nature and severity of adverse events
• Incidence, nature and severity of clinical laboratory test abnormalities

Efficacy/Secondary Outcome Parameters:

• Clinical remission defined as an endoscopy score of ≤ 1, a rectal bleeding score of 0, and an improvement or no change from baseline in the stool frequency score at the end of 2 weeks of treatment / withdrawal visit;
• Clinical response rate defined as the percentage of patients with a drop of ≥3 points from the baseline overall modified Mayo score;
• Patient defined response and remission rates;
• Change from baseline in the overall modified Mayo score (Disease Activity Index);
• Change from baseline in each of the 4 individual sub-scores of the modified Mayo score;
• Change from baseline in Investigator Assessment of UC Symptom Score (total and individual symptom scores)
• Change from baseline in IBDQ score (total and the 4 individual dimension scores)
• Proportion of patients with treatment failure;
• Change from baseline in serum lutein levels;
• Change from baseline in C-reactive protein (CRP), high sensitivity CRP (hs-CRP), erythrocyte sedimentation rate (ESR), fecal calprotectin (FCP), and fecal lactoferrin (FL).
• Change from baseline in exploratory biomarkers including: serum interleukin-2 (IL-2), IL-6, IL-8, interferon-gamma (IFN-gamma), tumor necrosis factor-alpha (TNF-α), transforming growth factor-beta (TGF-beta), IL-4, IL-10, IL-17, IL-23, human beta-Defensin-2 (hBD-2), malondialdehyde (MDA), lipoxin A4 (LXA4), glutathione (GSH), M30 and M65 apoptosomes in serum and biopsies, and plasma and urinary isoprostane levels.

Conditions

Left-Sided Ulcerative Colitis; Proctosigmoiditis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

PUR 0110 Rectal Enema 250 mg

Active treatment

Group Type: EXPERIMENTAL

PUR 0110 Rectal Enema 250 mg

Intervention Type: DRUG

PUR 0110 Rectal Enema 250 mg, once-daily, intrarectally

PUR 0110 Rectal Enema 500 mg

Active treatment

Group Type: EXPERIMENTAL

PUR 0110 Rectal Enema 500 mg

Intervention Type: DRUG

PUR 0110 Rectal Enema 500 mg, once-daily, intrarectally

PUR 0110 Rectal Enema 1000 mg

Active treatment

Group Type: EXPERIMENTAL

PUR 0110 Rectal Enema 1000 mg

Intervention Type: DRUG

PUR 0110 Rectal Enema 1000 mg, once-daily, intrarectally

Placebo Enema

Placebo comparator

Group Type: PLACEBO_COMPARATOR

Placebo Enema

Intervention Type: DRUG

Placebo Enema, once-daily, intrarectally

Interventions

PUR 0110 Rectal Enema 250 mg

PUR 0110 Rectal Enema 250 mg, once-daily, intrarectally

Intervention Type: DRUG

PUR 0110 Rectal Enema 500 mg

PUR 0110 Rectal Enema 500 mg, once-daily, intrarectally

Intervention Type: DRUG

PUR 0110 Rectal Enema 1000 mg

PUR 0110 Rectal Enema 1000 mg, once-daily, intrarectally

Intervention Type: DRUG

Placebo Enema

Placebo Enema, once-daily, intrarectally

Intervention Type: DRUG

Other Intervention Names

Active treatment arm; Active treatment arm; Active treatment arm; Placebo arm

Eligibility Criteria

Inclusion Criteria

1. Outpatient males and females between 18 and 75 years.

2. Females of child bearing potential must have a negative serum pregnancy test (beta-human chorionic gonadotropin) at screening and must be sexually inactive (abstinent) for 3 months prior to dosing and throughout the study or be using one of the following acceptable methods of contraception:

• barrier methods (condom, diaphragm with spermicide);
• Intrauterine device (IUD) in place for at least 3 months;
• surgical sterilization of the partner (vasectomy for at least 6 months); or
• hormonal contraceptives for at least 3 months prior to dosing. [Female subjects of childbearing potential must be advised to remain sexually inactive or maintain the same method of contraception for ≥7 days following the end of dosing of study treatment]

3. Patients newly diagnosed or with ongoing active distal ulcerative colitis of >3 months duration, confirmed by flexible sigmoidoscopy during screening, and extending 5 to 50 cm from the anal margin. Sigmoidoscopy must be conducted within not more than 3 +/- 1 days before the Baseline (Day 0) Visit.

4. Patients with ongoing active distal ulcerative colitis of ≥3 months duration must be on a stable dose of oral mesalamine (5-ASA) for ≥2 months before the Baseline (Day 0) Visit.

5. Modified Mayo Score (Disease Activity Index) of ≥5 to ≤10 at Baseline, including a sigmoidoscopic inflammation grade score of ≥2 and a rectal bleeding score ≥2.

6. Negative stool test at screening to rule out parasites, bacterial pathogens and Clostridium difficile.

7. Able and willing to fill in (maintain) daily diary cards from Day -7 to Day 21 of the study.

8. Able to provide voluntary written informed consent prior to initiation of screening, must be capable of following the verbal and written study instructions, and be able to commit to the return visits during the entire period of the study.

Exclusion Criteria

1. History or presence of clinically significant cardiovascular, pulmonary, hepatic, renal, hematological, gastrointestinal, endocrine, immunologic, dermatological, neurological, or psychiatric disease, that could compromise patient's ability to participate in the study, and/or interfere with absorption of the study drug or the interpretation of the study data.

2. Patients with a diagnosis of Crohn's disease.

3. Patients with a modified Mayo score of ≥11 at the Screening (Day -7 & Day -3) Visits.

4. Patients at immediate or significant risk of toxic megacolon; those with bowel stricture, colonic dysplasia, adenoma or carcinoma.

5. Use of botanical treatments and supplements for ulcerative colitis within 14 days prior to the Baseline Visit.

6. Patients with any enteric pathogens, ova or parasites, or Clostridium difficile toxin in stool.

7. Female patients with a positive pregnancy test or lactating at the Screening/Baseline Visits.

8. History of allergic reaction or hypersensitivity to spinach, spinach tablet, spinach powder or spinach extract; and to latex, molds and mushrooms.

9. History of gout, pseudogout or hyperuricemia, or kidney stones.

10. History of pseudoallergic hypersensitivity to the food color additives, tartrazine (E102), sunset yellow (E110) and FD & C Blue No.1 (Brilliant blue FCF; E133), allergic asthma, aspirin intolerance, and severe or multiple allergies.

11. Past medical history of significant gastrointestinal surgery including but not limited to colostomy, ileostomy, or previous colonic surgery other than appendectomy.

12. Patients with anatomical abnormalities of the colon, e.g., short bowel or other abnormalities.

13. Patients with any current infectious, ischemic, or immunologic disease with gastrointestinal involvement.

14. Patients with a history of failure to retain enemas.

15. Use of antibiotics for reasons related to the primary diagnosis or for other gastrointestinal-related conditions within 14 days of Baseline Visit.

16. Patients who used non-steroidal anti-inflammatory drugs (NSAIDs), including cyclooxygenase-2 (COX-2) inhibitors, within 14 days prior to Baseline Visit. Except aspirin ≤325 mg/day for cardiovascular prophylaxis.

17. Patients who used the following medications used for treating ulcerative colitis from the times indicated below to the end of Week 3 (Visit 6):

• Topical intrarectal corticosteroids or topical intrarectal mesalamine within 14 days of Baseline Visit;
• Systemic corticosteroids (oral or injectable, including adrenocorticotropic hormone [ACTH]) within 30 days of Baseline Visit;
• Immunosuppressant therapy (methotrexate, azathioprine, 6-mercatopurine or cyclosporine) within 60 days of Baseline Visit; and
• Biologic therapy (tumor necrosis factor-α inhibitors, monoclonal antibodies, etc.) within 90 days of Baseline Visit.

18. Patients with a history of active malignancy within the past 5 years except for squamous cell or basal cell cancers of the skin.

19. History of any clinical laboratory abnormality deemed significant by the Principal Investigator.

20. History of significant alcohol or drug abuse within one year prior to the Screening Visit.

21. Patients who tested positive at Screening for human immunodeficiency virus (HIV), hepatitis B surface antigen (HbsAg) or hepatitis C virus (HCV).

22. Exposure to any investigational or non-registered drug within 30 days prior to administration of study drug.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

PurGenesis Technologies Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Theophilus J Gana, MD, PhD

Role: STUDY_DIRECTOR

Devonian Health Group Inc.

Michael Rünzi, Prof. Dr. med.

Role: PRINCIPAL_INVESTIGATOR

Essen-Werden, Germany

Locations

PurGenesis Investigational Site

Jena, , Germany

PurGenesis Investigational Site

Köln-Merheim, , Germany

PurGenesis Investigational Site

Ludwigshafen, , Germany

PurGenesis Investigational Site

Minden, , Germany

PurGenesis Investigational Site

Oelde, , Germany

PurGenesis Investigational Site

Werden, , Germany

Countries

Germany

Other Identifiers

2009 017839 18

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

29PS1617

Identifier Type: OTHER

Identifier Source: secondary_id

PG09 PUR 0210 002

Identifier Type: -

Identifier Source: org_study_id