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Trial registered on ANZCTR
Registration number
ACTRN12614000171617
Ethics application status
Approved
Date submitted
3/02/2014
Date registered
11/02/2014
Date last updated
5/02/2018
Type of registration
Prospectively registered
Titles & IDs
Public title
A phase 1 study of dendrimer-docetaxel (DEP(TM) Docetaxel) in patients with advanced cancer.
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Scientific title
A phase 1 dose escalation study to evaluate the safety, tolerability and pharmacokinetics of DTX-SPL8783 (a docetaxel (DTX)-dendrimer conjugate) in patients with advanced solid tumours.
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Secondary ID [1]
284022
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Nil known
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Cancer
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Condition category
Condition code
Cancer
291406
291406
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0
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Any cancer
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
DEP(TM) Docetaxel (DTX-SPL8783) / Escalating doses by intravenous infusion, single dose once every cycle (cycle length of 3 weeks). Number of doses (i.e., cycles) and dosage amounts will depend on any toxicities occurring at each dose level. Starting dose of 10mg/m2, increased by 1.4 to 2 times at each dose level. Treatment will be continued until tumour progression, unacceptable toxicity or withdrawal from the study based on investigator discretion or patient decision.
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Intervention code [1]
288709
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Treatment: Drugs
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Comparator / control treatment
None - Dose escalation
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Determination of the maximum tolerated dose (MTD) as assessed by occurrence of dose limiting toxicities (DLT)
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Assessment method [1]
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Timepoint [1]
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During the first cycle of treatment (i.e. the first 3 weeks of treatment)
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Secondary outcome [1]
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General safety and tolerability profile, as determined by adverse events (AE) including ascites, pericardial effusions or pleural effusions. NCI Common Terminology Criteria for Adverse Events (CTCAE) version 4.0 will be utilised for AE assessment and reporting.
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Assessment method [1]
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Timepoint [1]
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Assessed at the end of each cycle of treatment (i.e., every 3 weeks)
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Secondary outcome [2]
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Tumour response according to Response Evaluation Criteria In Solid Tumors (RECIST) criteria
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Assessment method [2]
306664
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Timepoint [2]
306664
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Screening, and the end of Cycles 3, 6, 9 etc., while on study
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Secondary outcome [3]
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Pharmacokinetic profile tested via blood assay.
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Assessment method [3]
306665
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Timepoint [3]
306665
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Cycle 1 Days 1, 8 and 15, Cycle 2 Day 1
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Eligibility
Key inclusion criteria
Patients with histologically or cytologically confirmed advanced or metastatic cancer for which no standard or curative therapy exists; life expectancy of greater than 12 weeks; measurable or evaluable disease by RECIST.
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Allergy to docetaxel or other components of study therapy or compounds of similar chemical composition; uncontrolled intercurrent illness; participation in a study of an investigational agent within 30 days prior to first study therapy.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
Phase 1
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
12/02/2014
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Actual
12/03/2014
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Date of last participant enrolment
Anticipated
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Actual
11/01/2016
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Date of last data collection
Anticipated
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Actual
1/05/2017
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Sample size
Target
30
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Accrual to date
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Final
22
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,VIC
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Recruitment hospital [1]
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The Alfred - Prahran
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Recruitment hospital [2]
2850
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Royal Brisbane & Womens Hospital - Herston
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Recruitment hospital [3]
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Austin Health - Austin Hospital - Heidelberg
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Recruitment hospital [4]
3723
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Liverpool Hospital - Liverpool
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Recruitment postcode(s) [1]
7857
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3004 - Melbourne
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Recruitment postcode(s) [2]
8539
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4006 - Herston
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Recruitment postcode(s) [3]
8540
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3084 - Heidelberg
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Recruitment postcode(s) [4]
9544
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2170 - Liverpool
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Funding & Sponsors
Funding source category [1]
288649
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Commercial sector/Industry
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Name [1]
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Starpharma Pty Ltd
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Address [1]
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4-6 Southampton Crescent, Abbotsford, Victoria 3067
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Country [1]
288649
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Australia
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Primary sponsor type
Commercial sector/Industry
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Name
Starpharma Pty Ltd
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Address
4-6 Southampton Crescent, Abbotsford, Victoria 3067
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
287360
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Address [1]
287360
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Country [1]
287360
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
290500
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Alfred Health Human Ethics Committee
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Ethics committee address [1]
290500
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Ethics committee country [1]
290500
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Australia
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Date submitted for ethics approval [1]
290500
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Approval date [1]
290500
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22/01/2014
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Ethics approval number [1]
290500
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556/13
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Ethics committee name [2]
291503
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Austin Health Human Research Ethics Committee
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Ethics committee address [2]
291503
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Office for Research Level 8, Harold Strokes Building Austin Health 145 Studley Road Heidelberg Victoria 3084
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Ethics committee country [2]
291503
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Australia
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Date submitted for ethics approval [2]
291503
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Approval date [2]
291503
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22/05/2014
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Ethics approval number [2]
291503
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HREC-14/Austin/108
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Summary
Brief summary
The study is evaluating the safety, tolerability and pharmacokinetics of DTX-SPL8783 (a docetaxel (DTX)-dendrimer conjugate) in patients with advanced solid tumours. Who is it for? You may be eligible to join this study if you are aged over 18 years, have a histologically or cytologically confirmed advanced or metastatic cancer for which no standard or curative therapy exists, a life expectancy greater than 12 weeks, and your disease is measurable or evaluable by the Response Evaluation Criteria In Solid Tumours (RECIST). Trial details: Participants in this study will be administered DEP(TM) Docetaxel (DTX-SPL8783) via intravenous infusion in escalating doses once every 3 weeks. The number of doses and dosage amounts administered to participants are dependent on any toxicities occurring at each dose level. The starting dose is 10mg/m2, increased by 1.4 – 2 times at each dose level. Treatment will be continued until tumour progression, unacceptable toxicity or withdrawal from the study based on investigator discretion or patient decision.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Dr Jason Lickliter
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Address
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Nucleus Network
5th Floor, Burnet Tower, AMREP Precinct
89 Commercial Rd, Melbourne, Victoria 3004
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Country
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Australia
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Phone
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+61 3 90768900
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Jeremy Paull
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Address
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Starpharma Pty Ltd
4-6 Southampton Crescent, Abbotsford, Victoria 3067
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Country
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Australia
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Phone
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+61 3 85322736
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Fax
45975
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Email
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[email protected]
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Contact person for scientific queries
Name
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Jeremy Paull
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Address
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Starpharma Pty Ltd
4-6 Southampton Crescent, Abbotsford, Victoria 3067
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Country
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Australia
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Phone
45976
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+61 3 85322736
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Fax
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Dimensions AI
Recent advances in targeted drug delivery approaches using dendritic polymers
2015
https://doi.org/10.1039/c4bm00351a
Dimensions AI
Safety of Polysorbate 80 in the Oncology Setting
2018
https://doi.org/10.1007/s12325-018-0707-z
N.B. These documents automatically identified may not have been verified by the study sponsor.
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