- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07708116
First in Human Trial of CTX-187 in Healthy Volunteers and Chronically Infected Patients
13 juli 2026 uppdaterad av: Centauri Therapeutics Limited
A Phase 1 First-In-Human, Double-Blind, Single and Multiple Ascending Dose Trial to Evaluate Safety, Tolerability, Pharmacokinetics, and Immunogenicity of Intravenous Doses of CTX-187 in Healthy Volunteers Followed by Multiple Doses in Patients With a Bacterial Infection
The primary objective of this trial is to assess the safety and tolerability of single and multiple ascending intravenously (IV) infused doses of CTX-187 when administered to healthy adult male and female participants and participants with a bacterial infection (bronchiectasis participants chronically infected with P. aeruginosa).
Studieöversikt
Status
Rekrytering
Betingelser
Intervention / Behandling
Studietyp
Interventionell
Inskrivning (Beräknad)
104
Fas
- Fas 1
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studiekontakt
- Namn: Centauri Clinical Team
- Telefonnummer: Please use email
- E-post: clinical@centauritherapeutics.com
Studieorter
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Groningen, Nederländerna, 9728
- Rekrytering
- ICON Clinic, location GRQM
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Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Ja
Beskrivning
Inclusion Criteria
- Parts A and B: Healthy adult males and/or females, 18 to 65 years of age.
- Parts A and B: Body mass index (BMI): ≥18.0 and ≤32.0 kg/m^2 and weight >50 kg.
- Parts A and B: Good physical and mental health without clinically significant abnormalities.
- Part C: Adult males and/or females, 18 to 75 years of age.
- Part C: Prior clinical and computerized tomography diagnosis of bronchiectasis.
- Part C: P. aeruginosa in sputum, bronchoalveolar lavage or another airway sample at least once in the 12 months prior to screening and P. aeruginosa in sputum during screening, both of which should be at least 21 days apart.
- Part C: Otherwise in good physical and mental health without clinically significant abnormalities.
Exclusion Criteria
- Parts A and B: Previous participation in the current trial.
- Parts A and B: History or presence of significant cardiovascular, pulmonary, hepatic, renal, haematological, gastrointestinal, endocrine, immunologic, dermatologic, or neurological disease, including any acute illness or surgery within the past 3 months determined by the Investigator to be clinically relevant.
- Parts A and B: Participation in a drug trial within the previous 30 days before the first dose of trial drug or 5x elimination half-life, if known, whichever is longer.
- Part C: Known hypersensitivity to any reagents contained in CTX-187 or documented hypersensitivity reaction or anaphylaxis to any medication.
- Parts A, B and C: Known clinical diagnosis of cystic fibrosis, active allergic bronchopulmonary aspergillosis or active tuberculosis or nontuberculous mycobacterial infection; primary diagnosis of asthma or chronic obstructive pulmonary disease.
- Part C: Treatment with long term inhaled, systemic or nebulized anti-pseudomonal antibiotics which are newly initiated within the previous 3 months prior to screening.
- Part C: Receipt of anti-pseudomonal antibiotics for an exacerbation during the screening period.
- Part C: History or presence of unstable co-morbidities: cardiovascular, pulmonary, hepatic, renal, haematological, gastrointestinal, endocrine, immunologic, dermatologic, or neurological disease, including any acute illness or surgery within the past 3 months determined by the Investigator to be clinically relevant. Participants on stable doses of anti-hypertensive medications or statins may be included following discussion between the Investigator and the medical monitor.
- Part C: History of known or suspected Clostridioides difficile infection or diarrhoea within one week of recruitment, not resolved during the past 5 days.
- Part C: Participants with an acute exacerbation of bronchiectasis.
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Grundläggande vetenskap
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Dubbel
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: Part A (Single Ascending Dose [SAD]): CTX-187
Healthy participants will receive a single IV infusion of CTX-187 in escalating doses.
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CTX-187 will be administered via IV infusion.
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Placebo-jämförare: Part A (SAD): Placebo
Healthy participants will receive a single IV infusion of matching placebo.
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Placebo kommer att administreras via IV -infusion.
|
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Experimentell: Part B (Multiple Ascending Dose [MAD]): CTX-187
Healthy participants will receive multiple escalating doses of CTX-187 via IV infusion twice daily (BID) for 7 days.
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CTX-187 will be administered via IV infusion.
|
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Placebo-jämförare: Part B (MAD): Placebo
Healthy participants will receive matching placebo via IV infusion BID for 7 days.
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Placebo kommer att administreras via IV -infusion.
|
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Experimentell: Part C (MAD in Participants with a Bacterial Infection): CTX-187
Participants with a bacterial infection will receive multiple escalating doses of CTX-187 via IV infusion BID for 6 days (Days 2 to 7) with a single dose on Day 1 and Day 8.
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CTX-187 will be administered via IV infusion.
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Placebo-jämförare: Part C (MAD in Participants with a Bacterial Infection): Placebo
Participants with a bacterial infection will receive matching placebo via IV infusion BID for 6 days (Days 2 to 7) with a single dose on Day 1 and Day 8.
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Placebo kommer att administreras via IV -infusion.
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Number of Participants with Treatment-emergent Adverse Events (TEAEs)
Tidsram: Up to Day 28
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TEAEs include clinically significant abnormalities in electrocardiograms (ECGs), vital signs, clinical laboratory values and physical examination.
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Up to Day 28
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Sekundära resultatmått
Resultatmått |
Tidsram |
|---|---|
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Area Under the Concentration-time Curve (AUC) of CTX-187 in Plasma
Tidsram: Part A: Up to Day 2; Part B: Up to Day 8; Part C: Up to Day 9
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Part A: Up to Day 2; Part B: Up to Day 8; Part C: Up to Day 9
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Maximum Observed Plasma Concentration (Cmax) of CTX-187
Tidsram: Part A: Up to Day 2; Part B: Up to Day 8; Part C: Up to Day 9
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Part A: Up to Day 2; Part B: Up to Day 8; Part C: Up to Day 9
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Time to Attain Maximum Observed Plasma Concentration (tmax) of CTX-187
Tidsram: Part A: Up to Day 2; Part B: Up to Day 8; Part C: Up to Day 9
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Part A: Up to Day 2; Part B: Up to Day 8; Part C: Up to Day 9
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Terminal Elimination Half-life (t1/2) of CTX-187 in Plasma
Tidsram: Part A: Up to Day 2; Part B: Up to Day 8; Part C: Up to Day 9
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Part A: Up to Day 2; Part B: Up to Day 8; Part C: Up to Day 9
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Clearance (CL) of CTX-187
Tidsram: Part A: Up to Day 2; Part B: Up to Day 8; Part C: Up to Day 9
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Part A: Up to Day 2; Part B: Up to Day 8; Part C: Up to Day 9
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Volume of Distribution at Steady-state (Vss) of CTX-187
Tidsram: Part A: Up to Day 2; Part B: Up to Day 8; Part C: Up to Day 9
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Part A: Up to Day 2; Part B: Up to Day 8; Part C: Up to Day 9
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Number of Participants with Antidrug Antibodies (ADA) Against CTX-187 in Serum
Tidsram: Part A: Up to Day 2; Part B: Up to Day 8; Part C: Up to Day 9
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Part A: Up to Day 2; Part B: Up to Day 8; Part C: Up to Day 9
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Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
16 juni 2026
Primärt slutförande (Beräknad)
31 december 2027
Avslutad studie (Beräknad)
31 december 2027
Studieregistreringsdatum
Först inskickad
13 juli 2026
Först inskickad som uppfyllde QC-kriterierna
13 juli 2026
Första postat (Faktisk)
16 juli 2026
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
16 juli 2026
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
13 juli 2026
Senast verifierad
1 juli 2026
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- CTX-187-101
- 224842/Z/21/Z (Annat bidrag/finansieringsnummer: Wellcome Trust)
- Agmt dtd 1/30/2023 (Annat bidrag/finansieringsnummer: Germany's Federal Ministry of Education and Research)
- NNF23SA0088536 (Annan identifierare: Novo Nordisk Foundation (NNF))
- Agmt dtd 5/19/2025 (Annat bidrag/finansieringsnummer: The Ministry of Economy and Finance of Italy)
- CP-CA 25-79 (Annat bidrag/finansieringsnummer: EU/DG HERA/KfW)
- OTA No. 75A50122C00028 (Annat bidrag/finansieringsnummer: HHS/BARDA)
- 2026-525619-15-00 (Ctis)
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
NEJ
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Nej
Studerar en amerikansk FDA-reglerad produktprodukt
Nej
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