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.
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
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.
Response rate as assessed by RECIST every 8 weeks
Secondary outcomes (4)
Time to progression
Survival at 6 months and 1 year
Overall survival
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.
- First posted26 Nov 2007 (estimated)
- Study startFeb 2006
- Primary completionSep 2008
- Study completionOct 2010
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Melanoma (Skin)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Cambridge University Hospitals NHS Foundation Trust
- Sponsor type
- University, hospital or other
- Investigators
- Pippa Corrie, PhD, FRCP, Study chair, Cambridge University Hospitals NHS Foundation Trust
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
Study at a glance
From the registry record, last updated by the sponsor on 2 Aug 2013. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase II Study to Evaluate the Efficacy and Safety of PTK787 in Patients With Metastatic Cutaneous Melanoma
- ClinicalTrials.gov ID
- NCT00563823
- Acronym / sponsor ID
- CRCA-CCTC-CAMEL02
- Conditions
- Melanoma (Skin)
- Keywords
- stage IV melanoma, recurrent melanoma
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 34 participants (estimated)
- Lead sponsor
- Cambridge University Hospitals NHS Foundation TrustUniversity, hospital or other
- Study start
- Feb 2006
- Primary completion
- Sep 2008 (actual)
- Study completion
- Oct 2010 (actual)
- First posted
- 26 Nov 2007 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Masking
- None (open label)
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| vatalanib | Drug | – |
Primary outcome
Response rate as assessed by RECIST every 8 weeks
4 secondary outcomes
Time to progression
Survival at 6 months and 1 year
Overall survival
Toxicity as assessed by NCI CTCAE v3.0 at 2 weeks and then every 4 weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Aug 2013.
- Results publication: PubMed 20800475Cook 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.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Pippa Corrie, PhD, FRCP study chair
Cambridge University Hospitals NHS Foundation Trust
2 sites in 1 country: see every site and its status.
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.