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Phase 1b Clinical Study in Patients With Active Ulcerative Colitis (TP317-301)

16. september 2026 opdateret af: Thetis Pharmaceuticals LLC

A Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy Signal of TP-317 in Patients With Active Ulcerative Colitis

Purpose of study is to evaluate the safety, tolerability, pharmacokinetics of TP317 vs. placebo in adults with active ulcerative colitis. Participants will be randomly assigned to receive either daily oral tablets (8 tablets) of TP317 (80 mg) or an identical placebo pill. Study will include 2 colonoscopies, daily dosing (including at home and in clinic), safety assessments, diary and questionnaire completion and 5 in clinic visits.

Studieoversigt

Status

Ikke rekrutterer endnu

Betingelser

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

24

Fase

  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 65 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Diagnosis of UC with disease duration of at least 12 weeks prior to randomization

  • Evidence of active UC at Screening, defined by all of the following:

    1. MMS of 5 to 8, inclusive;
    2. ES ≥ 2;
    3. RBS of ≥ 1; and
    4. Evidence of active UC extending ≥15 cm from the anal verge via colonoscopy (confirmed by central read)
  • UCEIS score ≥ 4 with erosion/ulcer sub-score of ≥1 (confirmed by central read)

  • An inadequate response to, loss of response to, or intolerance to at least 1 of the following conventional therapies as defined below:

    1. Oral 5-ASA compounds
    2. Glucocorticoids (topical or systemic)
    3. Thiopurines
  • If receiving oral 5-aminosalicylates (5-ASAs) or oral corticosteroids (≤20 mg prednisolone equivalent) for treatment of their UC, they must be on a stable dose for at least 28 days prior to randomization

  • Previous exposure to a single biologic agent, JAK inhibitor, or S1P inhibitor is allowed (not required) if it was discontinued for reasons other than primary no response. Discontinuation must have been more than 8 weeks or 5 half-lives (whichever is longer) prior to first dose of study treatment.

Exclusion Criteria:

  • Severe extensive colitis as evidenced by:

    1. Likeliness to require hospitalization for medical care or surgical intervention of any kind for UC (e.g., colectomy) within 12 weeks after randomization
    2. Current evidence of fulminant colitis, toxic megacolon, or recent history (within 6 months prior to screening) of toxic megacolon, or bowel perforation
  • Has severe UC during as defined by ≥6 bloody stools per day AND at least 1 of the following during Screening:

    1. Pulse >90 bpm
    2. Oral temperature of >37.8 °C
    3. Hemoglobin <10.5 g/dL
    4. CRP of >30 mg/L
    5. Erythrocyte sedimentation rate >30 mm/h
  • Diagnosis of Crohn's disease (CD) or indeterminate colitis, microscopic colitis, ischemic colitis, radiation colitis, acute diverticulitis, or the presence or history of a fistula consistent with CD based on medical history

  • History of or current evidence of colonic dysplasia; or recent history (within 2 years prior to randomization). Note: If adenomatous polyps present, must be completely removed per routine practice prior to the study participant's first dose of investigational product.

  • History of colectomy (total or subtotal), ileoanal pouch, Kock pouch, or ileostomy; or is planning to undergo bowel surgery during the course of the study.

  • History of spontaneous gastrointestinal (GI) perforation (other than appendicitis or mechanical injury), or at significantly increased risk of GI perforation based on the Investigator's judgment

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Firedobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Aktiv komparator: Active TP317 80 mg

Participants will receive 8 tablets (80 mg) of TP317 daily, via oral administration for 12 weeks

8 tablets (80 mg) of TP317 oral tablets, taken once daily under fasted conditions for a total duration of 12 weeks.

Placebo komparator: Placebo

Participants will receive 8 tablets of matching Placebo daily, via oral administration for 12 weeks

Matching oral tablet containing no active ingredients, taken once daily for 12 weeks to maintain blinding.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Safety of TP317
Tidsramme: Collected from baseline through Week 12

Incidence, duration and severity of all adverse events (AEs).

Collected from baseline through Week 12
Safety of TP317
Tidsramme: Baseline through Week 12

Number of Participants with Clinically Significant Laboratory Abnormalities

Baseline through Week 12
Safety of TP317
Tidsramme: Baseline through Week 12

Number of Participants with Clinically Significant ECG Abnormalities

Baseline through Week 12
Safety of TP317
Tidsramme: Baseline to Week 12

Changes in 12-lead electrocardiogram parameters

Baseline to Week 12
Pharmacokinetics of TP317
Tidsramme: Baseline through Week 12

Maximum observed plasma concentration (Cmax) of TP317

Baseline through Week 12
Pharmacokinetics of TP317
Tidsramme: Baseline through Week 12

Time to maximum observed plasma concentration (Tmax) of TP317

Baseline through Week 12
Pharmacokinetics of TP317
Tidsramme: Baseline through Week 12

Area under the plasma concentration-time curve

Baseline through Week 12
Pharmacokinetics of TP317
Tidsramme: Baseline through Week 12

Plasma elimination half-life (t1/2) of TP317

Baseline through Week 12

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

16. september 2026

Primær færdiggørelse (Anslået)

29. juli 2027

Studieafslutning (Anslået)

29. august 2027

Datoer for studieregistrering

Først indsendt

20. juli 2026

Først indsendt, der opfyldte QC-kriterier

16. september 2026

Først opslået (Faktiske)

22. september 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

22. september 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

16. september 2026

Sidst verificeret

1. september 2026

Mere information

Begreber relateret til denne undersøgelse

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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