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NCT Number: NCT07767370

ND-12 Combined With H-6 for Adult Chronic Inflammatory Diarrhea

This is a randomized controlled trial to explore the efficacy and safety of ND-12 combined with H-6 for patients with chronic inflammatory diarrhea

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

The Second Affiliated Hospital of Nanjing Medical University

Nanjing, Jiangsu, 210011, China

Location status: Recruiting

Location contact

Faming Zhang, PhD

CONTACT

[email protected]

086-025-58509883

About this study

At least 36 subjects who meet all the inclusion criteria but do not meet any exclusion criteria will be enrolled in this study. They will be randomly assigned to the mesalazine group , ND-12, and the ND-12/H-6 group. Data of demographic characteristics, intestinal symptoms, medicine treatment usage and clinical outcomes will be collected. After treatment, they will enter the follow-up period for efficacy and safety evaluation.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects aged 18-75 years (inclusive), of any gender.
  • Meet any one of the following conditions:

1) Previously diagnosed ulcerative colitis, currently in the active phase; 2) Diagnosis of chronic diarrhoea: stool frequency ≥3 times per day or markedly higher than the subject's usual baseline; disease duration >4 weeks; recurrent diarrhoea with an interval of 2-4 weeks between episodes; loose stools (Bristol Stool Form Scale type 5, 6, or 7).

  • Faecal calprotectin >150 μg/g. 4.The subject or their legal representative provides informed consent by voluntarily signing the informed consent form, fully understands the study objectives, maintains effective communication with investigators, and is capable of understanding and complying with all requirements specified in this study protocol.

Exclusion criteria

Exclusion criteria

related to chronic diarrhoea

  • Presence of any of the following symptoms:
  • Fever ≥37.5°C;
  • Moderate-to-severe dehydration requiring intravenous fluid replacement;
  • Recurrent vomiting.
  • Diarrhoea caused by enteric pathogens (e.g., Clostridioides difficile, Salmonella typhi, etc.).
  • Underlying diseases that may trigger diarrhoea, including hyperthyroidism, gastrointestinal autonomic nervous dysfunction, gastrointestinal malignancy, Crohn's disease, history of colectomy (appendectomy, haemorrhoid surgery and fistula-in-ano surgery excluded), history of small-bowel resection (>20 cm of resected intestinal segment), etc.

Drug-related exclusion criteria

  • Suspected drug-induced diarrhoea (e.g., long-term use of laxatives, antibiotics, chemotherapeutic agents, etc.) where discontinuation of the offending drug is not feasible.
  • History of allergy to any component of mesalazine capsules, ND-12 capsules or H-6 capsules.
  • Anticipated need for prohibited medications during the study (e.g. antibiotics, antidiarrhoeals, antiemetics, antispasmodics, etc.).
  • Use of any investigational drug within 30 days prior to enrolment into this study.

Other gastrointestinal exclusion criteria

  • History of gastrectomy or vagotomy.
  • Known malabsorptive disorders include coeliac disease.
  • Known lactose intolerance.
  • Any suspected condition requiring abdominal surgery. Other exclusion criteria
  • Confirmed human immunodeficiency virus (HIV) positive status, known or suspected immunosuppression.
  • Known severe hepatic or renal insufficiency.
  • Past or current history of alcohol abuse and/or known substance abuse (cocaine, heroin, cannabis, etc.).
  • Any psychiatric condition impairing the subject's ability to understand the nature, scope and potential consequences of the study, and/or documented evidence of non-cooperation.
  • Pregnant or lactating women.

Treatment and study plan

Mesalazine

Drug

Take 4 melesalazine capsules each time, 3 times a day. Continue for 14 days.

ND-12

Drug

Take 1 ND-12 capsule and 3 blank capsules each time, 3 times a day. Continue for 14 days

ND-12/H-6

Drug

Take 1 ND-12 capsule and 3 H-6 capsules each time, 3 times a day. Continue for 14 days

Primary outcomes

  1. Fecal calprotectin of patients 14 days after treatment compared to the baseline level

    Time frame: baseline, 14 days post-drug administration

    The rate of change in fecal calprotectin levels of the subjects at 14 days compared to the baseline level

Secondary outcomes

  1. The proportion of subjects who achieved a clinical response on the 14th day

    Time frame: 14 days post-drug administration

    The proportion of subjects who achieved a clinical response on the 14th day(Fecal calprotectin decreased by ≥50% compared to the baseline or returned to normal <150 μg/g)

  2. The proportion of subjects achieving deep remission on the 14th day

    Time frame: 14 days post-drug administration

    The proportion of subjects achieving deep remission on the 14th day (Fecal calprotectin < 100 μg/g)

  3. Serum inflammatory factors after treatment

    Time frame: baseline, 14 days post-drug administration

    The changes in inflammatory factors (IL-1β, IL-10, TNF-α) in the blood of the subjects at 14 days compared to the baseline level

  4. The frequency of defecation after treatment

    Time frame: baseline, 7 days post-drug administration, 14 days post-drug administration, and 28 days post-drug administration

    The situation of the subjects' defecation frequency on the 7th, 14th, and 28th days compared to the baseline;

  5. The fecal consistency scores after treatment

    Time frame: baseline, 7 days post-drug administration, 14 days post-drug administration, and 28 days post-drug administration

    The changes in the fecal consistency scores (measured using the Bristol Fecal Form Scale) of subjects on the 7th, 14th, and 28th days compared to the baseline;

  6. The gastrointestinal symptom grading scores after treatment

    Time frame: baseline, 7 days post-drug administration, 14 days post-drug administration, and 28 days post-drug administration

    The gastrointestinal symptom grading scores (using the GSRS scoring scale) of subjects on the 7th, 14th, and 28th days compared with the baseline values

  7. The changes of gut microbiome and metabolome

    Time frame: baseline, 7 days post-drug administration

    Changes in the gut microbiome and metabolome of subjects on the 7th day compared with baseline

Study contacts

Contact information is provided by the study sponsor or research team.

Faming Zhang, PhD

CONTACT

[email protected]

086-025-58509883

Sponsors and collaborators

Lead sponsor

The Second Hospital of Nanjing Medical University

Other

Collaborators

  • Neurodawn Pharmaceutical Co., Ltd.

Registry information

Official study title

A Randomised, Controlled, Double-blind Exploratory Study of ND-12 Combined With H-6 in the Treatment of Adult Chronic Inflammatory Diarrhea

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Aug 17, 2026
Registry last updated
Aug 17, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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