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Study of Oral PQR309 in Patients With Advanced Solid Tumors

20. März 2019 aktualisiert von: PIQUR Therapeutics AG

Phase I Study of Oral PQR309 in Patients With Advanced Solid Tumors

This is an open-label, multi-center, non-randomized, dose escalation Phase 1 study evaluating safety, tolerability, PK (pharmacokinetics) and efficacy of PQR309 in the treatment of selected patients with advanced solid tumors.

Studienübersicht

Status

Abgeschlossen

Bedingungen

Intervention / Behandlung

Detaillierte Beschreibung

This is an open-label, multi-center, non-randomized, dose escalation Phase 1 study evaluating safety, tolerability, PK (pharmacokinetics)and efficacy of PQR309 in the treatment of selected patients with advanced solid tumors.

In the initial phase of the study, patients will be treated once daily until disease progression, unacceptable toxicity, patient's request for withdrawal, investigator judgment or death whichever comes first. Enrollment of an initial patient cohort of 3 or 6 patients will follow the traditional 3 + 3 dose escalation scheme to evaluate Dose Levels 1 - 5 with continuous q.d dosing schedule. Patients will be treated with PQR309 at starting Dose Level 1 enrolling exceptionally 6 patients (only applicable for continuous dosing schedule). Subsequent patient cohort(s) will be enrolled depending on the safety and tolerability of the initial cohort. If < 33% patients treated at Dose Level 1 (80 mg) experience Dose Limiting Toxicities (DLT - see definition below) by the end of first treatment cycle (21 days), next cohort of 3 patients will be enrolled and treated at Dose Level 2 of the continuous dosing schedule, if 2 or more treatment-related DLTs are observed at Dose Level 1, patients will be accrued to Dose Level -1. If 2 or more patients experience a DLT during dose Level 2 (120 mg), the dose of 100 mg will be explored next.The MTD is defined as the maximum dose level at which ≤ 1/6 patients have DLTs. After the MTD has been established with the continuous dosing schedule, the study will be expanded to evaluate the MTD of intermittent dosing schedules. Initially 2 additional dosing schedules, intermittent schedule A and B, will be evaluated in parallel. Patients will be assigned to the two schedules in an alternating manner.

Patients will be treated only within dose and schedule cohort they have been enrolled in. No within-patient dose escalation or alteration of dosing schedule will be allowed.Both schedules A and B will evaluate intermittent dosing in 21 day cycles:

Intermittent schedule A:

Two days of once daily PQR309 administration followed by no treatment for 5 days.

Intermittent schedule B:

PQR309 administration on Monday and Thursday. Same dose escalation procedures will apply to intermittent schedule evaluation as for the continuous schedule. Based on the overall evaluation of safety and tolerability, the PK (pharmacokinetics) data of the intermittent dosing schedules and the continuous schedule as well as PQR309 non-clinical data, evaluation of additional dosing schedules may be considered and investigated if agreed between sponsor and study investigators.

After the MTD has been established with the intermittent dosing schedules, the study will be expanded to evaluate the MTD of one selected schedule in patients with:

  • Solid tumors with PI3K/mTOR pathway activation
  • HPV positive HNSCC patients containing activating PIK3CA mutations Evaluation of the data from these cohorts will allow for more complete evaluation of tolerability, pharmacokinetics, and correlative endpoints as well as the preliminary clinical efficacy of PQR309.

Studientyp

Interventionell

Einschreibung (Tatsächlich)

70

Phase

  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Texas
      • Houston, Texas, Vereinigte Staaten, 77030
        • M.D. Anderson Cancer Center

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria

  1. Patients ≥ 18 years of age.
  2. Histologically or cytologically confirmed diagnosis of solid malignancy, for which no standard curative or life prolonging therapy is available.
  3. Have an ECOG Performance Status of ≤ 1. Refer to Appendix 1.
  4. Life expectancy of ≥ 12 weeks.
  5. Adequate bone marrow, liver, and renal functions, defined as:

    • Platelet count ≥ 100 x 109/L, absolute neutrophil count (ANC)

      ≥ 1.5 x 109/L, Hemoglobin ≥ 9 g/dL.

    • ALT and AST ≤ 2.5 upper limit normal (ULN), or < 5 x ULN if liver metastases are present; serum total bilirubin ≤ ULN or 1.5 x ULN if liver metastases are present or total 3 x ULN with direct bilirubin ≤ ULN in patients with well documented Gilbert Syndrome.
    • Serum Creatinine < 1.5 x ULN (upper limit of normal) or estimated creatinine clearance ≥ 60 mL/min, as calculated using method standard for the institution (Appendix 2).
  6. Glycated hemoglobin (HgbA1c) ≤ 7 %; Fasting Plasma Glucose (FPG) ≤ 7.0 mmol/L (125 mg/dL).
  7. Women of childbearing potential must have a negative pregnancy test (urine or serum) performed within 7 days prior to the start of study drug.
  8. Able and willing to swallow and retain oral medication.
  9. Subject or legal representative must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure.

    Expansion part:

  10. Patients must have known PI3K/mTOR pathway gene aberrations (from molecular profiling studies).
  11. Patients must have HPV positive HNSCC containing activating PIK3CA mutations.

Exclusion Criteria

  1. Concurrent or previous anti-cancer chemotherapy, immunotherapy or investigational agents < 3 weeks, or palliative radiation < 2 weeks prior to the first day of study treatment. Patients who receive gamma knife radiosurgery for brain metastases or whole brain radiation are eligible if gamma knife radiosurgery was performed > 2 weeks before treatment is started or whole brain radiation was performed > 4 weeks before treatment is started, and are clinically stable.
  2. Hormonal anticancer therapies except for LHRH antagonists or LHRH agonists in hormone-refractory prostate cancer
  3. Patient has a known hypersensitivity to any of the excipients of PQR309.
  4. Patient has had major surgery within 14 days prior to starting study drug or has not recovered from major side effects.
  5. Patients with poorly controlled diabetes mellitus, steroid-induced diabetes mellitus, HbA1c > 7%, or FPG > 7.0 mmol/L (125 mg/dL).
  6. Patients who are on (or will require) prolonged systemic corticosteroid treatment during the study, except for:

    • if receiving corticosteroids, patients must have been on a stable or decreasing dose of corticosteroids and no more than 1 mg of dexamethasone a day or equivalent, i.e. 6 mg prednisone or 25 mg hydrocortisone for at least 5 days prior to date of enrollment.
    • a short duration (< 5 days) of systemic corticosteroids e.g., of chronic obstructive pulmonary disease, or as an antiemetic corresponding at maximum to the anti-inflammatory potency of 4 mg dexamethasone for treatment;
    • topical applications for treatment of e.g., rash, inhaled sprays for treatment of e.g., obstructive airways diseases, eye drops or local Protocol No. PQR309-003 Protocol Amendment 3, 23 September 2015 PIQUR Therapeutics AG - Confidential Page 15 of 108 injections (e.g., intra-articular);
  7. Patients who have taken herbal medications and certain fruits within 7 days prior to starting study drug, see section 11.1.2.7.
  8. Patients who have other concurrent severe and/or uncontrolled medical conditions that would, in the investigator's judgment, contraindicate patient participation in the clinical study (e.g., active or uncontrolled severe infection, chronic active hepatitis, immuno-compromised, acute or chronic pancreatitis, uncontrolled high blood pressure, interstitial lung disease, etc.).
  9. Patient has a known history of HIV infection (testing not mandatory).
  10. Patient has any of the following cardiac abnormalities:

    • History of, or current, documented congestive heart failure (New York Heart Association functional classification III - IV), documented cardiomyopathy.
    • Left Ventricular Ejection Fraction (LVEF) < 40% as determined by Multiple Gated Acquisition (MUGA) scan or echocardiogram (ECHO).
    • Myocardial infarction ≤ 6 months prior to enrolment.
    • Unstable angina pectoris.
    • Serious uncontrolled cardiac arrhythmia.
    • Symptomatic pericarditis.
  11. Patient has impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of study drug.
  12. Concomitant treatment with medicinal products that increase the pH (reduce acidity) of the upper gastrointestinal tract, including, but not limited to, proton-pump inhibitors (e.g. omeprazole), H2-antagonists (e.g. ranitidine) and antacids. Patients may be enrolled in the study after a wash-out period sufficient to terminate their effect.
  13. Patient has a history of non-compliance to medical regimen or inability to grant consent.
  14. Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive Human Chorionic Gonadotropin (hCG) laboratory test (> 5 mIU/mL). Patients with elevated hCG at baseline that is judged to be related to the tumor are eligible if hCG levels do not show the expected doubling when repeated 5 - 7 days later, or pregnancy has been ruled out by vaginal ultrasound.
  15. Patient who does not apply highly effective contraception during the study from screening until 90 days after discontinuing study treatment Protocol No. PQR309-003 Protocol Amendment 3, 23 September 2015 PIQUR Therapeutics AG - Confidential Page 16 of 108 (see section 11.3).
  16. Patients have any of the following mood disorders as judged by the Investigator or a Psychiatrist, or who meets the cut-off score of ≥ 12 the PHQ-9 or a cut-off of ≥ 15 in the GAD-7 mood scale, respectively, or selects a positive response of '1, 2, or 3' to question number 9 regarding potential for suicidal thoughts in the PHQ-9 (independent of the total score of the PHQ-9) see Appendix 4.

    • Medically documented history of or active major depressive episode, bipolar disorder (I or II), obsessive-compulsive disorder, schizophrenia, a history of suicidal attempt or ideation, or homicidal ideation (immediate risk of doing harm to others).
    • ≥ CTCAE Grade 3 anxiety.
  17. Patients with a history of interstitial

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: PQR309
Different dose Evaluation (continous and intermittent) 20-160mg daily
Intervention of this drug may include safety, tolerability, PK (pharmacokinetics) and efficacy
Andere Namen:
  • PI3K/mTOR/AKT Inhibitor

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
To identify the Maximum Tolerated Dose (MTD) of PQR309 administered in different (continuous and intermittent) dosing schedules. To evaluate efficacy of PQR309 in selected patient population: • Solid tumors with PI3K/mTOR activation • Human Papilloma
Zeitfenster: In average 1 year
MTD based on the rate of dose-limiting toxicities. The MTD is defined as the maximum dose level at which ≤ 1/6 patients have dose limiting toxicities (DLTs).
In average 1 year
Objective response rate (ORR) according to the response evaluation• Solid tumors with PI3K/mTOR activation • Human Papilloma Virus (HPV) positive Head and neck squamous cell carcinoma (HNSCC) containing activating PIK3CA mutations
Zeitfenster: in average 2 years
Expansion part criteria in solid tumors (RECIST), version 1.1
in average 2 years

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Number of patients with adverse Events and serious adverse events
Zeitfenster: Cycle1 on Day1,8,15, Cycle 2 and subsequent cycles on Day 1, End of the treatment up to 3 days and as follow up 30 days after last dosing
Continous Dosing and intermittent dosing "2days on/5days off
Cycle1 on Day1,8,15, Cycle 2 and subsequent cycles on Day 1, End of the treatment up to 3 days and as follow up 30 days after last dosing
Number of patients with adverse Events and serious adverse events
Zeitfenster: Assessment on Day 1 after basline, Cycle1 on Day 8,15, Cycle 2 and subsequent cycles on Day 1, End of the treatment up to 3 days and as follow up 30 days after last dosing
"Monday/ Thursday"
Assessment on Day 1 after basline, Cycle1 on Day 8,15, Cycle 2 and subsequent cycles on Day 1, End of the treatment up to 3 days and as follow up 30 days after last dosing
Physical examination according to ECOG (Eastern Cooperative Oncology Group) Performance Status
Zeitfenster: Cycle 1 on Day 8,15, Cycle 2 and subsequent cycles on Day1 , end of treatment up to 3 days after
Continous Dosing
Cycle 1 on Day 8,15, Cycle 2 and subsequent cycles on Day1 , end of treatment up to 3 days after
Physical examination according to ECOG (Eastern Cooperative Oncology Group) Performance Status
Zeitfenster: Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1 , end of treatment up to 3 days after
Intermittent Dosing "2days on/5days off"
Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1 , end of treatment up to 3 days after
Physical examination according to ECOG (Eastern Cooperative Oncology Group) Performance Status
Zeitfenster: Assessment on Day1,2, Cycle 1 on Day 4,8,9,15
Intermittent Dosing "Monday/ Thursday"
Assessment on Day1,2, Cycle 1 on Day 4,8,9,15
Change in Pulse Rate
Zeitfenster: Assessment on Day 3 after baseline, Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Continous Dosing
Assessment on Day 3 after baseline, Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Change in Pulse Rate
Zeitfenster: Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Intermittent Dosing "2 days on/5days off"
Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Change in Pulse Rate
Zeitfenster: Assessment on Day1,2,Cycle 1 on Day 4,8,9,15
Intermittent Dosing "Monday/ Thursday"
Assessment on Day1,2,Cycle 1 on Day 4,8,9,15
Change in Temperature
Zeitfenster: Assessment on Day 3 after baseline, Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Continous Dosing
Assessment on Day 3 after baseline, Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Change in Temperature
Zeitfenster: Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Intermittent Dosing "2days on/5days off"
Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Change in Temperature
Zeitfenster: Assessment on Day1,2,Cycle 1 on Day 4,8,9,15
Intermittent Dosing " Assessment on Day1,2,Cycle 1 on Day 4,8,9,15
Assessment on Day1,2,Cycle 1 on Day 4,8,9,15
Change in Respiratory Rate
Zeitfenster: Assessment on Day 3 after baseline, Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Continous Dosing
Assessment on Day 3 after baseline, Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Change in Respiratory Rate
Zeitfenster: Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Intermittent Dosing "2days on/5days off"
Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Change in Respiratory Rate
Zeitfenster: Assessment on Day1,2,Cycle 1 on Day 4,8,9,15
Intermittent Dosing " Monday/ Thursday"
Assessment on Day1,2,Cycle 1 on Day 4,8,9,15
Change in Blood Pressure
Zeitfenster: Assessment on Day 3 after baseline, Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Continous Dosing
Assessment on Day 3 after baseline, Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Change in Blood Pressure
Zeitfenster: Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Intermittent Dosing "2days on/5days off"
Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Change in Blood Pressure
Zeitfenster: Assessment on Day1,2,Cycle 1 on Day 4,8,9,15
Intermittent Dosing "Monday/ Thursday"
Assessment on Day1,2,Cycle 1 on Day 4,8,9,15
Change in Blood Body Weight
Zeitfenster: Assessment on Day 3 after baseline, Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Continous Dosing
Assessment on Day 3 after baseline, Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Change in Blood Body Weight
Zeitfenster: Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Intermittent Dosing "2days on/5days off"
Cycle 1 on Day 1,8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Change in Blood Body Weight
Zeitfenster: Assessment on Day1,2,Cycle 1 on Day 4,8,9,15
Intermittent Dosing "Monday/ Thursday"
Assessment on Day1,2,Cycle 1 on Day 4,8,9,15
Change in ECG
Zeitfenster: Assessment on Day 3 after baseline, Cycle 1 on Day 8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Continous Dosing
Assessment on Day 3 after baseline, Cycle 1 on Day 8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Change in ECG
Zeitfenster: After Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Intermittent Dosing "2days on/5days off" and "Monday/ Thursday"
After Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Depression test (PHQ-9)
Zeitfenster: After Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Continous Dosing
After Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Depression test (PHQ-9)
Zeitfenster: Cycle 1 on Day 8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Intermittent Dosing "2days on/5days off" and "Monday/ Thursday"
Cycle 1 on Day 8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Generalized anxiety disorder mood scale score (GAD7)
Zeitfenster: Cycle 1 on Day 8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Continous Dosing and Intermittent Dosing "2days on/5days off" and "Monday/ Thursday"
Cycle 1 on Day 8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Changes in routine blood chemistry
Zeitfenster: Cycle 1 on Day 1, 8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Continous Dosing and Intermittent Dosing "2days on/5days off"
Cycle 1 on Day 1, 8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Changes in routine blood chemistry
Zeitfenster: Assessment on Day 1 after baseline, Cycle 1 on Day 8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Intermittent Dosing "Monday/ Thursday"
Assessment on Day 1 after baseline, Cycle 1 on Day 8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Changes of hematology
Zeitfenster: Cycle 1 on Day 1, 8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Continous Dosing and Intermittent Dosing "2days on/5days off"
Cycle 1 on Day 1, 8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Changes of hematology
Zeitfenster: Assessment on Day 1 after baseline, Cycle 1 on Day 8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Intermittent Dosing "Monday/ Thursday"
Assessment on Day 1 after baseline, Cycle 1 on Day 8,15, Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Changes of insulin/Glucose/ C-peptide
Zeitfenster: Assessment on Day 3, ,2,1 after baseline, Cycle 1 on Day 1, Cycle 2 and subsequent cycles on Day1
Continous Dosing
Assessment on Day 3, ,2,1 after baseline, Cycle 1 on Day 1, Cycle 2 and subsequent cycles on Day1
Changes of insulin/Glucose/ C-peptide
Zeitfenster: Assessment on Day 3, 2,1 after baseline, Cycle 8,9,15 on Day 1
" Intermittent Dosing "2days on/5days off""
Assessment on Day 3, 2,1 after baseline, Cycle 8,9,15 on Day 1
Changes of insulin/Glucose/ C-peptide
Zeitfenster: Assessment on Day 1,2 after baseline, Cycle1 on Day 4, 8,9,15
" Intermittent Dosing "Monday/ Thursday"
Assessment on Day 1,2 after baseline, Cycle1 on Day 4, 8,9,15
Changes of haemostasis
Zeitfenster: Cycle 1 on Day 1, 8, 15 Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Continous Dosing and Intermittent Dosing "2days on/5days off"
Cycle 1 on Day 1, 8, 15 Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Changes of haemostasis
Zeitfenster: Assessment on Day 1 after baseline, Cycle 1 on Day 1,15 Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Intermittent Dosing "Monday/ Thursday"
Assessment on Day 1 after baseline, Cycle 1 on Day 1,15 Cycle 2 and subsequent cycles on Day1, end of treatment up to 3 days after last medication
Determination of Cmax
Zeitfenster: Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,15, Cycle 2 on Day1
Continous Dosing
Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,15, Cycle 2 on Day1
Determination of Cmax
Zeitfenster: Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,9,15
Intermittent Dosing "2days on/5days off"
Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,9,15
Determination of Cmax
Zeitfenster: Assessment on Day 1,2 after baseline, Cycle 1 on Day 4,8,9,15
Intermittent Dosing "Monday/ Thursday"
Assessment on Day 1,2 after baseline, Cycle 1 on Day 4,8,9,15
Determination of AUC 0-24
Zeitfenster: Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,15, Cycle 2 on Day1
Continous Dosing
Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,15, Cycle 2 on Day1
Determination of AUC 0-24
Zeitfenster: Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,9,15
Intermittent Dosing "2days on/5days off"
Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,9,15
Determination of AUC 0-24
Zeitfenster: Assessment on Day 1,2 after baseline, Cycle 1 on Day 4,8,9,15
Intermittent Dosing "Monday/ Thursday"
Assessment on Day 1,2 after baseline, Cycle 1 on Day 4,8,9,15
Determination of tmax
Zeitfenster: Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,15, Cycle 2 on Day1
Continous Dosing
Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,15, Cycle 2 on Day1
Determination of tmax
Zeitfenster: Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,9,15
Intermittent Dosing "2days on/5days off"
Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,9,15
Determination of tmax
Zeitfenster: Assessment on Day 1,2 after baseline, Cycle 1 on Day 4,8,9,15
Intermittent Dosing "Monday/ Thursday"
Assessment on Day 1,2 after baseline, Cycle 1 on Day 4,8,9,15
Determination of AUClast (area under the curve)
Zeitfenster: Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,15, Cycle 2 on Day1
Continous Dosing
Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,15, Cycle 2 on Day1
Determination of AUClast
Zeitfenster: Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,9,15
Intermittent Dosing "2days on/5days off"
Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,9,15
Determination of AUClast
Zeitfenster: Assessment on Day 1,2 after baseline, Cycle 1 on Day 4,8,9,15
Intermittent Dosing "Monday/ Thursday"
Assessment on Day 1,2 after baseline, Cycle 1 on Day 4,8,9,15
Determination of AUC0-∞
Zeitfenster: Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,15, Cycle 2 on Day1
Continous Dosing
Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,15, Cycle 2 on Day1
Determination of AUC0-∞
Zeitfenster: Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,9,15
Intermittent Dosing "2days on/5days off"
Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,9,15
Determination of AUC0-∞
Zeitfenster: Assessment on Day 1,2 after baseline, Cycle 1 on Day 4,8,9,15
Intermittent Dosing "Monday/ Thursday"
Assessment on Day 1,2 after baseline, Cycle 1 on Day 4,8,9,15
Determination of t 1/2
Zeitfenster: Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,15, Cycle 2 on Day1
Continous Dosing
Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,15, Cycle 2 on Day1
Determination of t 1/2
Zeitfenster: Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,9,15
Intermittent Dosing "2days on/5days off"
Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,9,15
Determination of t 1/2
Zeitfenster: Assessment on Day 1,2 after baseline, Cycle 1 on Day 4,8,9,15
Intermittent Dosing "Monday/ Thursday"
Assessment on Day 1,2 after baseline, Cycle 1 on Day 4,8,9,15
Determination of RAC (Accumulation Ratio)
Zeitfenster: Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,15, Cycle 2 on Day1
Continous Dosing
Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,15, Cycle 2 on Day1
Determination of RAC (Accumulation Ratio)
Zeitfenster: Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,9,15
Intermittent Dosing "Monday/ Thursday"
Assessment on Day 3,2,1 after baseline, Cycle 1 on Day 8,9,15
Determination of RAC (Accumulation Ratio)
Zeitfenster: Assessment on Day 1,2 after baseline, Cycle 1 on Day 4,8,9,15
Intermittent Dosing "Monday/ Thursday"
Assessment on Day 1,2 after baseline, Cycle 1 on Day 4,8,9,15
Determine Time to Response (TTR)
Zeitfenster: up to 2 years
Efficacy
up to 2 years
Determine Duration of Response (DOR)
Zeitfenster: baseline and on Day 1 of every subsequential cycle which can be up to 24 months
Defined as the time from the date of the first confirmed response to the first documentation of relapse or progressive disease, whichever occurs first
baseline and on Day 1 of every subsequential cycle which can be up to 24 months
Time to Treatment Failure (TTF)
Zeitfenster: Tumor Measurement preferably with a ruler and/or MRI scans e.g. and incorporated clinical signs will be assesses at baseline and on Day 1 of every subsequential cycle which can be up to 24 months
Defined as the time from study entry to any treatment failure including disease progression or discontinuation of treatment for any reason (e.g., disease progression, AE, patient preference, initiation of new treatment without documented progression, death)
Tumor Measurement preferably with a ruler and/or MRI scans e.g. and incorporated clinical signs will be assesses at baseline and on Day 1 of every subsequential cycle which can be up to 24 months
Determine Progression Free Survival (PFS)
Zeitfenster: baseline and on Day 1 of every subsequential cycle which can be up to 24 months
Defined as the time from study entry to progression or death due to any cause
baseline and on Day 1 of every subsequential cycle which can be up to 24 months
1- year Survival Rate
Zeitfenster: baseline and on Day 1 of every subsequential cycle which can be up to 36 months
Defined as the time from study entry to death as a result of any cause at 1-year cutoff date
baseline and on Day 1 of every subsequential cycle which can be up to 36 months

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Hauptermittler: Alex Adjei, Mayo Clinic
  • Hauptermittler: Martin Forster, University College London Hospitals
  • Studienleiter: Mateusz Opyrchal, Roswell Park Cancer Institute
  • Hauptermittler: Filip Janku, MD Anderson Cancer
  • Hauptermittler: Afshin Dowlati, University Hospitals Cleveland Medical Center
  • Hauptermittler: Jordi Rodon, Vall d'Hebron University Hospital
  • Hauptermittler: Sarah Bladgen, Chruchill Hospital
  • Hauptermittler: Andreas Wicki, Basel university hospital

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

21. März 2019

Primärer Abschluss (Tatsächlich)

21. März 2019

Studienabschluss (Tatsächlich)

21. März 2019

Studienanmeldedaten

Zuerst eingereicht

19. Mai 2015

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

26. Juni 2015

Zuerst gepostet (Schätzen)

29. Juni 2015

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

22. März 2019

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

20. März 2019

Zuletzt verifiziert

1. März 2019

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Schlüsselwörter

Andere Studien-ID-Nummern

  • PQR309-003

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

UNENTSCHIEDEN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Ja

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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