- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT01922752
To Determine the Maximum Tolerated Dose of Oral CEP-37440 in Patients With Advanced or Metastatic Solid Tumors
5 november 2021 uppdaterad av: Teva Branded Pharmaceutical Products R&D, Inc.
An Open-Label Study to Determine the Maximum Tolerated Dose of Oral CEP-37440 Administered as a Single Agent in Patients With Advanced or Metastatic Solid Tumors
The primary objective is to determine the maximum tolerated dose (MTD), safety, and tolerability of oral CEP-37440 administered daily to patients with advanced or metastatic solid tumors.
Studieöversikt
Studietyp
Interventionell
Inskrivning (Faktisk)
32
Fas
- Fas 1
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
Illinois
-
Chicago, Illinois, Förenta staterna
- Teva Investigational Site 10689
-
-
Pennsylvania
-
Philadelphia, Pennsylvania, Förenta staterna
- Teva Investigational Site 10687
-
-
Texas
-
San Antonio, Texas, Förenta staterna
- Teva Investigational Site 10686
-
-
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
18 år och äldre (Vuxen, Äldre vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Beskrivning
Inclusion Criteria:
- Patients must have histologic or cytologic evidence of a solid neoplasm for which no standard therapy is available, or have progressed despite standard therapy, or are intolerant to standard therapy.
- Patients must have evidence of recurrent, locally advanced, or metastatic disease.
- Patients can either have had no prior anticancer therapy, multiple lines of either prior chemotherapy/biologic therapy/experimental therapy or, if the patient has anaplastic lymphoma kinase (ALK)-positive non-small cell lung cancer (NSCLC), prior crizotinib.
- Patients must have a predicted life expectancy of more than 3 months.
- Patients must have presence of at least 1 lesion that is measurable or evaluable using RECIST v1.1.
- Patients must have an ECOG performance score of 0, 1, or 2.
- Patients with central nervous system (CNS) metastases will be allowed on this study. Patients may have received surgical and/or radiation treatment. The metastases must be neurologically stable, on or off corticosteroids. Patients can have low level, asymptomatic brain lesions that do not require surgical/radiation intervention acutely. Patients with symptomatic lesions with impending neurologic compromise should be appropriately treated with high dose steroids/radiation and may be re-evaluated for this study when neurologically stable.
- Patients must have completed any prior anticancer treatment and must have recovered from any acute toxicities. The period between the last dose of prior treatment and the first dose of study drug treatment must be at least 1 week for radiotherapy and at least 2 to 3 weeks for all other modalities of therapy including chemotherapy, monoclonal antibody therapy, immunotherapy, other investigational drugs, or other kinase inhibitors.
- Other criteria apply.
Exclusion Criteria:
- The patient has ongoing or active infection requiring parenteral antibiotics.
- The patient has uncontrolled hypertension despite adequate therapy (ie, systolic blood pressure higher than 150 mm Hg or diastolic blood pressure higher than 90 mm Hg found on 2 separate occasions separated by 1 week).
- The patient has uncontrolled diabetes mellitus (despite therapeutic intervention) and occurrence of more than 2 episodes of ketoacidosis in the 12 months prior to the first dose of study drug.
- The patient has an active second malignancy other than curatively resected basal cell carcinoma of the skin, squamous cell carcinoma of the skin, in situ carcinoma of the cervix, or other cancers for which they are treated with curative intent, and no known active disease in the 3 years prior to enrollment.
- The patient has a primary brain tumor. Patients may have brain metastases from another primary site.
- The patient has QTcF interval greater than 450 msec, has a known history of QTcF prolongation, is taking medications known to prolong QTcF, or has a history of torsade de pointes.
- The patient has a prior ALK-inhibitor-related toxicity or any other prior therapy-related acute toxicity that has not resolved prior to the first dose of study drug.
- Other criteria apply.
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: CEP-37440
|
CEP-37440 will be supplied as 25 mg and 100 mg capsules and will be orally administrated daily. Patients will be enrolled sequentially in dose escalating cohorts to receive CEP-37440 until a maximum tolerated dose has been defined. |
Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
|---|---|
|
Response Evaluation Criteria in Solid Tumors (RECIST v1.1)
Tidsram: 8 months
|
8 months
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Time to Response (TTR)
Tidsram: 8 months
|
The time interval from the date of first dose to the first documented response (complete or partial response)
|
8 months
|
|
Number of participants with adverse events
Tidsram: From signing of the informed consent to the end of the follow-up visit (approximately Month 10)
|
From signing of the informed consent to the end of the follow-up visit (approximately Month 10)
|
|
|
Time to Progression (TTP)
Tidsram: 8 months
|
The time interval from date of first dose to first documented disease progression
|
8 months
|
|
Progression-free Survival (PFS)
Tidsram: 10 months
|
Time interval from date of first does to first documented disease progression or death from any cause (whichever occurs first)
|
10 months
|
|
Time to New Metastases (TTNM)
Tidsram: 8 months
|
Time interval from date of first dose to first documented new metastatic lesion not reported at baseline
|
8 months
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
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
1 juli 2013
Primärt slutförande (Faktisk)
1 september 2015
Avslutad studie (Faktisk)
1 december 2015
Studieregistreringsdatum
Först inskickad
12 augusti 2013
Först inskickad som uppfyllde QC-kriterierna
12 augusti 2013
Första postat (Uppskatta)
14 augusti 2013
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
12 november 2021
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
5 november 2021
Senast verifierad
1 november 2021
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- C37440/1108
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .