Safety Study Of A Liposomal Docetaxel Formulation In Patients With Solid Tumors Who Have Failed Previous Therapies

Study Overview

Safety Study of a Liposomal Docetaxel Formulation in Patients With Solid Tumors Who Have Failed Previous Therapies

The purpose of this study is to determine the safety profile, including the maximum tolerated dose (MTD), of ATI-1123 a liposomal formulation of docetaxel, in the treatment of cancer patients with advanced solid tumors.

The majority of advanced stage human cancers are fatal if not treated promptly and aggressively. Standard treatments include chemotherapy, radiation therapy and surgery. Docetaxel, the active ingredient in ATI-1123 and the FDA approved drug Taxotere, is a chemotherapy given by IV to patients to treat various types of cancers. Docetaxel is a poorly water soluble semi-synthetic taxane analog commonly used in the treatment of a variety of solid tumors including non-small cell lung, prostate, breast, gastric and head and neck cancer. Because of its poor water solubility it is formulated with co-solvents that can potentially contribute to treatment related adverse events such as hypersensitivity. Current taxane formulations often complicate drug delivery and can alter both pharmacokinetic and toxicity profiles. Results from nonclinical evaluations show that ATI-1123 retains the antineoplastic activity of docetaxel while removing the need for unwanted solvents like Tween 80. The administration of ATI-1123 versus other docetaxel chemotherapy formulations is expected to reduce hypersensitivity reactions (redness, swelling, itching at the infusion site), eliminate the requirement for premedications, have a broader therapeutic index, and enhance systemic docetaxel exposure.

Solid Tumor
Breast Cancer
Ovarian Cancer
Pancreatic Cancer
Non-Small Cell Lung

DRUG: ATI-1123 (active drug = docetaxel)

ATI1123-101

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates	Results Reporting Dates	Study Record Updates
First Submitted 2009-12-30	Results First Submitted N/A	Last Update Submitted that met QC Criteria 2012-09-04
First Submitted that Met QC Criteria 2009-12-30	Results First Submitted that Met QC Criteria N/A	Last Update Posted (ESTIMATED) 2012-09-06
First Posted (ESTIMATED) 2009-12-31	Results First Posted N/A	Last Verified 2012-09

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Design Details

Primary Purpose:
Treatment

Allocation:
Non Randomized

Interventional Model:
Single Group

Masking:
None

Arms and Interventions

Participant Group/Arm	Intervention/Treatment
EXPERIMENTAL: ATI-1123	DRUG: ATI-1123 (active drug = docetaxel) Dose escalation starting at 15 mg/m2 given once every 3 weeks via IV

Participant Group/Arm

Intervention/Treatment

EXPERIMENTAL: ATI-1123

DRUG: ATI-1123 (active drug = docetaxel)

Dose escalation starting at 15 mg/m2 given once every 3 weeks via IV

Primary Outcome Measures	Measure Description	Time Frame
To determine the (MTD) and (DLTs) of ATI-1123 administered every 3 weeks, over a range of doses in patients with advanced solid tumors.		Duration of study
To establish the dose recommended for future phase II studies with ATI-1123.		End of Study

Secondary Outcome Measures	Measure Description	Time Frame
To establish the pharmacokinetics of intravenously administered ATI-1123.		Cycle 1 (various time points within the cycle)
To observe patients for any evidence of antitumor activity of ATI-1123 by objective radiographic assessment.		Every 8 weeks

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.

Ages Eligible for Study:
ALL

Sexes Eligible for Study:
18 Years

Accepts Healthy Volunteers:

Understand and sign a written IRB-approved informed consent form.
Have a histologically confirmed solid tumor.
Have progressive disease following standard/approved chemotherapy or have no appropriate alternative therapy available.
Have one or more tumors measurable or evaluable as outlined by modified RECIST or evaluable by CT or MRI scan.
Have an ECOG performance status of ≤ 2.
Have a life expectancy of at least 3 months.
Be ≥ 18 years old.
Have a negative pregnancy test (if female of childbearing potential)
Demonstrate acceptable hepatic function:
Bilirubin ≤ upper limit of normal (ULN)
AST (SGOT) and ALT (SGPT) ≤ 2.5 times ULN
Demonstrate acceptable renal function:
Serum creatinine ≤ 1.5 x ULN, OR calculated creatinine clearance ≥ 60 mL/min/1.73 m2 for patients with creatinine levels above institutional normal (Calculated according to the Cockroft and Gault formula)
Demonstrate acceptable hematologic status:
Absolute neutrophil count ≥ 1500/mm3
Platelet count ≥ 100,000/mm3 (measured within 72 hours prior to initial dose)
Hemoglobin ≥ 9 g/dL
Demonstrate acceptable coagulation status:
PT or INR within 1.5x ULN
PTT within 1.5x ULN
Have recovered from prior treatments (eg, surgery, radiation, chemotherapy, investigational therapies) sufficiently prior to Day 1 so that, in the opinion of the Investigator and/or Medical Monitor, the protocol objectives would not be compromised.
Agree to use an effective contraceptive method (hormonal or barrier method; or abstinence) for the duration of the study and for 30 days after the last dose (for men and women of child-producing potential).

Have New York Heart Association Class III or IV cardiac disease, myocardial infarction within the past 6 months prior to Day 1, unstable arrhythmia, or evidence of ischemia on electrocardiogram (ECG).
Have a seizure disorder requiring anticonvulsant therapy.
Have active CNS metastasis. Patients with a history of CNS metastases will be eligible if they have been treated and are stable without symptoms for 4 weeks after completion of treatment, with image documentation required, and must be either off steroids or on stable dose of steroids for ≥ 1 week prior to enrollment.
Have severe, chronic obstructive pulmonary disease with hypoxemia.
Have active, uncontrolled bacterial, viral, or fungal infections requiring systemic therapy.
Are pregnant or nursing.
Have undergone radiation therapy, surgery, chemotherapy, or investigational therapy within 28 days prior to study entry (6 weeks for nitrosoureas or Mitomycin C).
Are unwilling or unable to comply with procedures required in this protocol.
Have a known history of infection with HIV, hepatitis B, or hepatitis C.
Have a serious nonmalignant disease that, in the opinion of the Investigator and/or the Medical Monitor, could compromise protocol objectives.
Are currently receiving any other investigational agent.
Have exhibited allergic reactions to docetaxel, or a similar structural compound, biological agent, or formulation.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

PRINCIPAL_INVESTIGATOR: Anthony W Tolcher, MD, South Texas Accelerated Research Therapeutics (START)

Publications

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

No publications available

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