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Melanoma (Skin)Phase 2NCT00563823

Vatalanib in Treating Patients With Metastatic Cutaneous Melanoma That Cannot be Removed by Surgery

A Phase 2 study testing vatalanib in people with Melanoma (Skin), run by Cambridge University Hospitals NHS Foundation Trust at 2 sites in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

RATIONALE: Vatalanib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. PURPOSE: This phase II trial is studying how well vatalanib works in treating patients with metastatic cutaneous melanoma that cannot be removed by surgery. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Melanoma (Skin)
What is being tested?
vatalanib
How many people
34 participants
Where
2 sitesUnited Kingdom
Study dates
Feb 2006to Oct 2010
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

DISEASE CHARACTERISTICS:

  • Histologically or cytologically confirmed metastatic cutaneous melanoma
  • Unresectable disease
  • Measurable disease, defined as ≥ 1 bidimensionally measurable lesion by clinical or radiological techniques (i.e., chest x-ray, CT scan, or conventional MRI scan) using RECIST criteria
  • No history or presence of CNS disease (i.e., primary brain tumor, malignant seizures, clinically symptomatic CNS metastases, or carcinomatous meningitis)

PATIENT CHARACTERISTICS:

  • ECOG performance status 0-2
  • Life expectancy ≥ 12 weeks
  • Hemoglobin ≥ 10 g/dL
  • Platelet count ≥ 100,000/mm^3
  • WBC ≥ 3,000/mm^3
  • ANC ≥ 1,500/mm^3
  • Bilirubin ≤ 1.5 x upper limit of normal (ULN)
  • Alkaline phosphatase ≤ 3 x ULN (≤ 5 if liver metastases are present)
  • Transaminases ≤ 3 x ULN (≤ 5 if liver metastases are present)
  • Creatinine ≤ 1.5 x ULN or creatinine clearance ≥ 50 mL/min
  • Total urinary protein ≤ 500 mg by 24-hour urine collection
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective barrier contraception
  • No history of other malignant disease except adequately treated nonmelanoma skin cancer or carcinoma in situ of the cervix
  • No other serious or uncontrolled illness which, in the opinion of the investigator, precludes study entry
  • No medical or psychiatric condition that precludes giving informed consent
  • No history of renal disease (e.g., glomerulonephritis) or renal vascular disease
  • No acute or chronic active liver disease (e.g., hepatitis or cirrhosis)
  • No concurrent severe and/or uncontrolled medical conditions that would compromise participation in the study, including any of the following:
  • Uncontrolled high blood pressure, history of labile hypertension, or history of poor compliance with an antihypertensive regimen
  • Unstable angina pectoris
  • Symptomatic congestive heart failure
  • Myocardial infarction within the past 6 months
  • Serious uncontrolled cardiac arrhythmia
  • Uncontrolled diabetes
  • Active or uncontrolled infection
  • No impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of vatalanib including, but not limited to, any of the following conditions:
  • Ulcerative disease
  • Uncontrolled nausea
  • Vomiting
  • Diarrhea which might result in malabsorption
  • Any known malabsorption syndrome
  • Bowel obstruction
  • Inability to swallow the capsules/tablets

PRIOR CONCURRENT THERAPY:

  • Recovered from all prior therapy
  • Prior adjuvant therapy allowed
  • Prior radiotherapy allowed
  • Measurable target lesions must not have been irradiated
  • No more than one line of prior systemic therapy for advanced melanoma
  • More than 4 weeks since prior chemotherapy, immunotherapy, or investigational agent
  • More than 2 weeks since prior surgery
  • No concurrent warfarin or other similar oral anticoagulants that are metabolized by the cytochrome p450 system
  • Concurrent heparin allowed
  • Concurrent radiotherapy for symptomatic disease is allowed, provided the lesions being irradiated contribute ≤ 20% of the sum of the longest diameter for all target lesions being used to determine response

Trial locations and contacts

2 sites in 1 country.

United Kingdom2 sites
  • Addenbrooke's Hospital

    Cambridge, England, CB2 2QQ

  • Leicester Royal Infirmary

    Leicester, England, LE1 5WW

Other trials in United Kingdom

About this study

Official title: A Phase II Study to Evaluate the Efficacy and Safety of PTK787 in Patients With Metastatic Cutaneous Melanoma

RATIONALE: Vatalanib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor.

PURPOSE: This phase II trial is studying how well vatalanib works in treating patients with metastatic cutaneous melanoma that cannot be removed by surgery.

Read the detailed description

OBJECTIVES:

Primary

  • To determine the response rate in patients with unresectable metastatic cutaneous melanoma treated with vatalanib.

Secondary

  • To determine the time to progression in these patients.
  • To determine the 6-month and 1-year survival of these patients.
  • To determine the overall survival of these patients.
  • To determine the safety and toxicity of this drug in these patients.

OUTLINE: This is a multicenter study.

Patients receive oral vatalanib twice daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

After completion of study therapy, patients are followed at 8 weeks and then periodically thereafter.

Conditions
Melanoma (Skin)
Being tested
vatalanib
Keywords
stage IV melanoma, recurrent melanoma
Medical subject headings
Melanoma

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • vatalanibDrug

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Response rate as assessed by RECIST every 8 weeks

Secondary outcomes (4)
  1. Time to progression

  2. Survival at 6 months and 1 year

  3. Overall survival

  4. Toxicity as assessed by NCI CTCAE v3.0 at 2 weeks and then every 4 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Nov 2007 (estimated)
  2. Study startFeb 2006
  3. Primary completionSep 2008
  4. Study completionOct 2010

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Masking
None (open label)
Enrolment
34 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00563823
Sponsor's protocol ID
CRCA-CCTC-CAMEL02
Other IDs
CDR0000576458, EU-20787, EUDRACT-2005-004710-33, CCLG-Camel-02, ISRCTN00191981
Status last verified
Apr 2008
First submitted
22 Nov 2007
Last updated
2 Aug 2013
Results posted
No

Publications

  • Cook N, Basu B, Biswas S, Kareclas P, Mann C, Palmer C, Thomas A, Nicholson S, Morgan B, Lomas D, Sirohi B, Mander AP, Middleton M, Corrie PG. A phase 2 study of vatalanib in metastatic melanoma patients. Eur J Cancer. 2010 Oct;46(15):2671-3. doi: 10.1016/j.ejca.2010.07.014. Epub 2010 Aug 25.

    PubMed 20800475

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing vatalanib in people with Melanoma (Skin), run by Cambridge University Hospitals NHS Foundation Trust at 2 sites in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 Aug 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Response rate as assessed by RECIST every 8 weeks. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00563823, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Aug 2013.

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