- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01977638
Phase 1 Trial of CXD101 in Patients With Advanced Cancer
17. oktober 2022 oppdatert av: Oxford University Hospitals NHS Trust
Phase 1 Study to Assess Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of CXD101 Given Orally (Twice Daily Dosing for 5 Consecutive Days in a 21-day Period) in Patients With Advanced Malignancies Expressing the Biomarker HR23B
The purpose of this study is to determine the highest dose of CXD101 (a novel histone deacetylase inhibitor) that can be safely administered to patients with advanced tumours.
The study will also investigate the use of HR23B expression in tumour as a biomarker of response to treatment with CXD101.
Patients with solid tumours, lymphoma and myeloma can be considered for this study.
Studieoversikt
Detaljert beskrivelse
Patients will be treated with CXD101 administered orally starting at 1mg twice a day (ie: 2mg/day).
Dose escalation will proceed according to a standard 3+3 phase 1 scheme.
Adverse experiences will be evaluated according to the NCI Common Terminology Criteria for Adverse Events, version 4.0.
Dose escalation will continue until dose limiting toxicity is encountered in >1/3rd of patients at any dose level.
The dose level below this will be determined to be the maximum tolerated dose.
Patients will be treated, at the discretion of the Principal Investigator, until disease progression, unacceptable toxicity or the withdrawal of consent.
At the maximum tolerated dose a further 20 patients, defined by tumour HR23B expression will be enrolled.
Studietype
Intervensjonell
Registrering (Faktiske)
51
Fase
- Fase 1
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Oxfordshire
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Oxford, Oxfordshire, Storbritannia, OX3 7LE
- Oxford University Hospitals NHS Trust
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Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år og eldre (Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- Age ≥ 18 years.
- Life expectancy of at least 12 weeks.
- ECOG performance score of ≤ 1
- Histologically or cytologically confirmed malignant tumour with the potential to benefit from HDAC inhibitor therapy.
- High HR23B expressing tumour sample on IHC (expansion cohort only).
- Evaluable disease.
- The patient is willing and able to comply with the protocol for the duration of the study, including scheduled follow-up visits and examinations.
- Patients must have recovered from effects of prior treatments, including surgeries (persistent grade 1 toxicities are permitted at the discretion of the Chief Investigator).
- Female patients with reproductive potential must have a negative urine or serum pregnancy test within 14 days prior to start of trial. Both women and men must agree to use a medically acceptable method of contraception throughout the treatment period and for 16 weeks after discontinuation of treatment. Oral contraception and parenteral hormonal contraceptives (patches, injectables and implants) that may be affected by enzyme-inducing drugs should only be used in combination with a barrier method. All males with partners of childbearing potential or whose partners are pregnant must use barrier contraception for the duration of dosing and for 16 weeks post-dosing.
- Able to give written (signed and dated) informed consent.
- Haematological and biochemical indices within acceptable ranges as detailed in study protocol.
Exclusion Criteria:
- Pregnant or breast-feeding women or women of childbearing potential unless effective methods of contraception are used.
- Other psychological, social or medical condition, physical examination finding or a laboratory abnormality that the Investigator considers would make the patient a poor trial candidate or could interfere with protocol compliance or the interpretation of trial results.
- Patients who are known to be serologically positive for Hepatitis B, Hepatitis C or HIV.
- Radiotherapy (except for palliative reasons), endocrine therapy, immunotherapy or use of other investigational agents within 28 days prior to trial entry (or a longer period depending on the defined characteristics of the agents used). Limited field radiotherapy to an isolated lesion in bone or soft tissue must be completed 2 weeks prior to trial entry.
- Patients must not receive any concurrent anti-cancer therapy, including investigational agents, while on-study. Patients may continue the use of bisphosphonates for bone disease or corticosteroids providing the dose is stable before and during the trial.
- Major surgery within 4 weeks of starting the study.
- Co-existing active infection requiring parenteral antibiotics or serious concurrent illness deemed clinically significant.
- Patients with known brain metastases, unless these are shown to be stable (symptomatically and/or radiologically) over a period of 2 months or more.
- History of refractory nausea and vomiting, chronic GI diseases (eg: inflammatory bowel disease) or significant bowel resection that would preclude adequate absorption of oral medication.
- Patients who are unable to swallow oral medication.
- Patients with corrected QT interval >450msec.
- Persistent grade 2 or greater toxicities from any cause.
- Previous treatment with a HDAC inhibitor.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: CXD101
Dose escalation study of CXD101 administered orally twice daily for 5 consecutive days in every 21 day cycle.
Starting dose 1mg twice daily (2mg/day).
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Capsules, administered orally
Andre navn:
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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To determine the maximum tolerated dose of CXD101 administered twice daily for 5 consecutive days every 21 days
Tidsramme: 18 months
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18 months
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Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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To determine the pharmacokinetic (PK) profile of CXD101 following single and multiple dosing
Tidsramme: 18 months
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18 months
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To enable a preliminary assessment of the anti-tumour activity of CXD101
Tidsramme: 24 months
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24 months
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To evaluate the tissue expression of the biomarker HR23B
Tidsramme: 24 months
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24 months
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To assess the pharmacodynamic effect of CXD101
Tidsramme: 24 months
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24 months
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Publikasjoner og nyttige lenker
Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
14. februar 2014
Primær fullføring (Faktiske)
8. oktober 2019
Studiet fullført (Faktiske)
14. oktober 2022
Datoer for studieregistrering
Først innsendt
5. november 2013
Først innsendt som oppfylte QC-kriteriene
5. november 2013
Først lagt ut (Anslag)
7. november 2013
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
18. oktober 2022
Siste oppdatering sendt inn som oppfylte QC-kriteriene
17. oktober 2022
Sist bekreftet
1. oktober 2021
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- CXD101-0901
- 2009-012743-42 (EudraCT-nummer)
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
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