Phase II Study Of Oral PHA-848125AC In Patients With Thymic Carcinoma

Thymic Carcinoma Clinical Trial

Official title:

Phase II Study Of Oral PHA-848125AC In Patients With Thymic Carcinoma Previously Treated With Chemotherapy

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01011439
• Other study ID #: CDKO-125a-006
• Secondary ID: 2009-014338-79
• Status: Terminated
• Phase: Phase 2
• Start date: February 22, 2010
• Est. completion date: December 17, 2018

Study information

• Verified date: January 2019
• Source: Tiziana Life Sciences, PLC
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The intent of the study is to assess the antitumor activity of PHA-848125AC as second-line treatment in patients with recurrent or metastatic, unresectable thymic carcinoma previously treated with chemotherapy.

Description:

The Simon's optimal 2 stage design is adopted for this single-arm, open-label, multicenter phase II clinical trial of PHA-848125AC administered to patients with recurrent or metastatic, unresectable thymic carcinoma previously treated with chemotherapy (only one prior systemic therapy allowed). The intent of the study is to assess the antitumor activity of PHA-848125AC and ultimately to improve the outcome of patients with thymic carcinoma who have already exploited one chemotherapy option. The primary end point for this study is a progression free survival rate of 3 months.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 72
• Est. completion date: December 17, 2018
• Est. primary completion date: May 31, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically or cytologically proven diagnosis of unresectable B3 thymoma or thymic carcinoma recurrent or progressing after prior chemotherapy (only one prior systemic therapy allowed)

• Presence of measurable disease

• Age >=18 years

• ECOG performance status 0-1

• Negative pregnancy test (if female in reproductive years)

• Use of effective contraceptive methods if men and women of child producing potential

• Adequate liver function Total Serum Bilirubin <=1.5 x upper limit of normal (ULN) Transaminases (AST/ALT) <=2.5ULN (if liver metastases are present, then <=5ULN is allowed) ALP <=2.5ULN (if liver and/or bone metastases are present, then <=5ULN is allowed)

• Adequate renal function Serum Creatinine <=ULN or Creatinine Clearance calculated by Cockcroft and Gault's formula > 60 mL/min.

• Adequate hematologic status ANC >=1,500cells/mm3 Platelet Count >=100,000cells/mm3 Hemoglobin >=9.0g/dL

• Two weeks must have elapsed since completion of prior chemotherapy, minor surgery, radiotherapy (provided that no more than 25% of bone marrow reserve has been irradiated)

• Resolution of all acute toxic effects of any prior treatments to NCI CTC (Version 3.0) grade <=1

Exclusion Criteria:

• Any of the following in the past 6 months: myocardial infarction, uncontrolled cardiac arrhythmia, unstable angina, coronary/peripheral artery bypass graft, symptomatic congestive heart failure, cerebrovascular accident or transient ischemic attack, pulmonary embolism, deep vein thrombosis

• Grade >1 retinopathy

• Known brain metastases

• Known active infections

• Pregnant or breast feeding women

• Diabetes mellitus uncontrolled

• Gastrointestinal disease that would impact on drug absorption

• Patients under treatment with anticoagulants or with coagulation disorders or with signs of hemorrhage at baseline

• Patients with previous history or current presence of neurological disorders, including epilepsy (although controlled by anticonvulsant therapy), Parkinson's disease and extra-pyramidal syndromes

• Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that make the patient inappropriate for entry into this study

Related Conditions & MeSH terms

• Carcinoma
• Thymic Carcinoma
• Thymoma

Intervention

Drug:
• Milciclib Maleate
150 mg/day once daily, for 7 consecutive days (days 1 to 7) followed by 7 days of rest (days 8 to 14) in a 2-week cycle. Number of cycles: until disease progression or unacceptable toxicity.

Locations

Country	Name	City	State
France	Hopital Larrey	Toulouse Cedex
France	Institut de cancerologie Gustave Roussy	Villejuif Cedex
Italy	Fondazione IRCCS Istituto Nazionale dei Tumori di Milano	Milano	(mi)
Italy	Azienda Ospedaliera San Luigi Gonzaga	Orbassano
United States	NIH, Center for Cancer Research, Medical Oncology	Bethesda	Maryland
United States	TGen Clinical Research Services at Scottsdale Healthcare	Scottsdale	Arizona

Sponsors (1)

Lead Sponsor	Collaborator
Tiziana Life Sciences, PLC

Countries where clinical trial is conducted

United States,  France,  Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression-free Survival Rate at 3 Months	The proportion of successes (i.e. patients alive and progression free at 3 months since treatment start) out of the total number of evaluable patients	3 months since treatment start
Secondary	Confirmed Objective Response Rate (ORR)	Point and 95% confidence interval estimates was calculated for the objective tumor response rate (confirmed CRs or PRs). The determination of antitumor efficacy was based on objective tumor assessments made according to the RECIST guideline (version 1.1) The analysis was performed in the evaluable population.	Assessments were made every 6 weeks from start date until PD to a maximum duration of 242 weeks or until PD.
Secondary	Disease Control Rate	Point and 95% confidence interval estimates was calculated for the disease control rate (confirmed CRs / PRs and SD>/= 6 weeks). The analysis was performed in the evaluable populations.	Assessments were made every 6 weeks from start date until PD to a maximum duration of 242 weeks or until PD.
Secondary	Progression-free Survival	The length of time during and after the treatment of a disease, such as cancer, that a patient lives with the disease but it does not get worse. In a clinical trial, measuring the progression-free survival is one way to see how well a new treatment works.	Assessments were made every 6 weeks from start date until PD to a maximum duration of 242 weeks or until PD.
Secondary	Duration of Response	Assessed in patients achieving a confirmed objective tumor response by RECIST version 1.1 criteria.	Assessments were made every 6 weeks from start date until PD to a maximum duration of 242 weeks or until PD.
Secondary	Overall Survival	The length of time from the start of treatment for a disease, such as cancer, to the date in which the patients diagnosed with the disease were still alive.	Every 6 weeks during Follow-Up until PD or new therapy start; every 6 months thereafter, up to 2 years from the last dose of study drug.
Secondary	Overall Safety Profile (Adverse Events (NCI CTCAE) and Hematological and Blood Chemistry Parameters)	The adverse events (AEs) were coded with the Medical Dictionary for Regulatory Activities (MedDRA) and their severity graded according to the NCI Common Terminology Criteria for Adverse Events (CTCAE) version 3.0. The following subsets of AEs were considered: serious AEs, AEs with CTCAE grade 3-5, AEs with a relationship to study treatment classified by the Investigator as possible or probable or definite and AEs reported as leading to discontinuation from treatment.; Laboratory test values were graded according to the NCI CTCAE scale, v3.0, whenever possible. For each laboratory test included in the NCI CTCAE system, the incidence of abnormalities was evaluated by considering the worst occurrence for each patient throughout the whole treatment period.	Adverse events: from date treatment consent signed to 28 days after last dose of study drug; hematology/blood chemistry tests: at baseline and between Day 11-14 of each cycle of a total of 135 two-week cycles.