ClinicalTrials.gg
CompletedNCT02100371Updated Jul 11, 2017

Study of BMS-833923 in Two Specific Patients With Basal Cell Nevus Syndrome

An interventional study of BMS-833923 in Basal Cell Nevus Syndrome, sponsored by University Health Network, Toronto. Completed at 1 site in Canada. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-07-11.

Sponsored by University Health Network, Toronto · Not applicable, Interventional, and Treatment

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Phase
Not applicable
Study type
Interventional
Enrollment
2
Allocation
Not applicable
Ages
18 Years and older
Sex
Female
01

Study summary

This is an extension study of Protocol CA194002 to allow 2 specific participants with basal cell nevus syndrome in the CA194002 study at Princess Margaret Cancer Centre who are still benefitting from the study drug BMS-833923 to continue receiving the study drug. This study will continue to evaluate the safety and tolerability of BMS-833923 in these participants.

Read the detailed description

The purpose of this study is to evaluate the safety and tolerability of BMS-833923 administered on an extension protocol in subjects with basal cell nevus syndrome (BCNS). This is an extension study of Protocol CA194002 to allow 2 specific participants with BCNS in the CA194002 study at Princess Margaret Cancer Centre who are still benefitting from the study drug BMS-833923, to continue receiving the study drug. In this open-label extension protocol, no new subjects will be recruited. The two BCNS subjects from Protocol CA194002 (subjects CA194002-1-14 and CA194002-1-25) will continue to receive BMS-833923 at the dose and schedule administered on CA194002 until fulfilling protocol criteria for discontinuation. These patients are receiving different doses: one being 60mg once every 2 weeks, and the other is receiving 300mg once daily. This study will continue to evaluate the safety and tolerability of BMS-833923 in these participants.

02

Conditions studied

  • Basal Cell Nevus Syndrome

Keywords

  • BMS-833923
  • CA194002
03

In context

Basal Cell Nevus Syndrome

35 studies on the registry are indexed under Basal Cell Nevus Syndrome; 4 are open to participants now.

This study's enrollment of 2 is below the median of 24 across 25 interventional studies indexed under Basal Cell Nevus Syndrome.

Browse Basal Cell Nevus Syndrome studies →

Lead sponsor

University Health Network, Toronto is the lead sponsor of 1,438 studies on the registry; 297 are open to participants now.

Of its 17 completed or terminated interventional studies of FDA-regulated products, 3 (18%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Signed consent
  • Two specific study participants enrolled on protocol CA194002 at Princess Margaret Cancer Centre and remain on BMS-833923 at the time of study entry
  • Women, age 18 years and above
  • Agree to use methods to prevent pregnancy, not pregnant or breastfeeding

Exclusion criteria

Exclusion Criteria:

  • Known symptomatic
  • A serious uncontrolled medical disorder or active infection, which would impair the ability of the patient to receive protocol therapy
  • Gastrointestinal disease or surgery that could impact the absorption of study drug
  • Inability to swallow oral medication
  • Inability to be venipunctured and/or tolerate venous access
  • Uncontrolled or significant cardiovascular
  • Any other medical, psychiatric and/or social reason
  • Have , HepB, or HepC
  • Exposure to and immunotherapy concurrently with study treatment and up to 3 months
  • Acceptable physical and laboratory test findings
  • History of allergy to compounds chemically-related
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Brain metastases

Cancer deposits in the brain from a cancer that started elsewhere in the body (CNS metastases include the spinal cord).

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HIV

The human immunodeficiency virus, which weakens the immune system.

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Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

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05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
2 participants (actual)

Study arms

  • Experimental
    BMS-833923

    BMS-833923, by mouth, at the dose and schedule administered while enrolled in CA194002.

    Drug: BMS-833923

Interventions

  • BMS-833923, by mouth, at the dose and schedule administered while enrolled in CA194002.

    Also known as: XL139

06

What researchers measure

Primary outcomes

  1. Frequency of side effects experienced per participant

    Time frame: From date of first study drug dose taken for this study until participant discontinuation, assessed up to 5 years

Secondary outcomes

  1. Length of time participants' disease does not worsen

    Time frame: From date of first study drug dose taken for this study until the date of first documented progression or date of death from any cause, whichever comes first, accessed up to 5 years

07

Study locations

1 site
  • Princess Margaret Cancer Centre
    Toronto, Ontario M5G 2M9, Canada
08

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Feb 2014, a primary completion of May 2017 and a completion of May 2017. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 28, 2014
First posted
Mar 31, 2014
Start
Feb 2014
Primary completionActual
May 2017
CompletionActual
May 2017
Last update
Jul 11, 2017
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 11, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02100371
Responsible party
Sponsor
First posted
Mar 31, 2014
Start date
Feb 2014
Primary completion
May 2017
Completion
May 2017
Last update
Jul 11, 2017

Study contacts

Lillian Siu, M.D.
principal investigator · Princess Margaret Cancer Centre

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2017. You cannot join it, but the record below documents what was studied.

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Discussion

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Studies of the drug tested here: BMS-833923

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