- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07834515
Phase 1b Clinical Study in Patients With Active Ulcerative Colitis (TP317-301)
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.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Tipo di studio
Iscrizione (Stimato)
Fase
- Fase 1
Contatti e Sedi
Contatto studio
- Nome: Head of Clinical Development Operations
- Numero di telefono: 203-936-8936
- Email: bpaperiello@thetispharma.com
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
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:
- MMS of 5 to 8, inclusive;
- ES ≥ 2;
- RBS of ≥ 1; and
- 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:
- Oral 5-ASA compounds
- Glucocorticoids (topical or systemic)
- 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:
- Likeliness to require hospitalization for medical care or surgical intervention of any kind for UC (e.g., colectomy) within 12 weeks after randomization
- 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:
- Pulse >90 bpm
- Oral temperature of >37.8 °C
- Hemoglobin <10.5 g/dL
- CRP of >30 mg/L
- 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
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Quadruplicare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Comparatore attivo: 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. |
|
Comparatore placebo: 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. |
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Safety of TP317
Lasso di tempo: Collected from baseline through Week 12
|
Incidence, duration and severity of all adverse events (AEs). |
Collected from baseline through Week 12
|
|
Safety of TP317
Lasso di tempo: Baseline through Week 12
|
Number of Participants with Clinically Significant Laboratory Abnormalities |
Baseline through Week 12
|
|
Safety of TP317
Lasso di tempo: Baseline through Week 12
|
Number of Participants with Clinically Significant ECG Abnormalities |
Baseline through Week 12
|
|
Safety of TP317
Lasso di tempo: Baseline to Week 12
|
Changes in 12-lead electrocardiogram parameters |
Baseline to Week 12
|
|
Pharmacokinetics of TP317
Lasso di tempo: Baseline through Week 12
|
Maximum observed plasma concentration (Cmax) of TP317 |
Baseline through Week 12
|
|
Pharmacokinetics of TP317
Lasso di tempo: Baseline through Week 12
|
Time to maximum observed plasma concentration (Tmax) of TP317 |
Baseline through Week 12
|
|
Pharmacokinetics of TP317
Lasso di tempo: Baseline through Week 12
|
Area under the plasma concentration-time curve |
Baseline through Week 12
|
|
Pharmacokinetics of TP317
Lasso di tempo: Baseline through Week 12
|
Plasma elimination half-life (t1/2) of TP317 |
Baseline through Week 12
|
Collaboratori e investigatori
Sponsor
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- TP317-301
Informazioni su farmaci e dispositivi, documenti di studio
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Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .