Register a trial

Registering a new trial?

To achieve prospective registration, we recommend submitting your trial for registration at the same time as ethics submission.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT04145349




Registration number
NCT04145349
Ethics application status
Date submitted
29/10/2019
Date registered
30/10/2019

Titles & IDs
Public title
CAMPFIRE: A Study of Ramucirumab (LY3009806) in Children and Young Adults With Desmoplastic Small Round Cell Tumor
Scientific title
A Randomized, Open-Label Phase 1/2 Study Evaluating Ramucirumab in Pediatric Patients and Young Adults With Relapsed, Recurrent, or Refractory Desmoplastic Small Round Cell Tumor
Secondary ID [1] 0 0
J1S-MC-JV01
Secondary ID [2] 0 0
17305
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Desmoplastic Small Round Cell Tumor 0 0
Condition category
Condition code
Cancer 0 0 0 0
Sarcoma (also see 'Bone') - soft tissue
Cancer 0 0 0 0
Children's - Other

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - Ramucirumab
Treatment: Drugs - Cyclophosphamide
Treatment: Drugs - Vinorelbine

Experimental: Ramucirumab + Cyclophosphamide + Vinorelbine - Ramucirumab given intravenously (IV), Cyclophosphamide given orally and vinorelbine given IV.

Active comparator: Cyclophosphamide + Vinorelbine - Cyclophosphamide given orally and vinorelbine given IV.


Treatment: Drugs: Ramucirumab
Administered IV

Treatment: Drugs: Cyclophosphamide
Administered orally

Treatment: Drugs: Vinorelbine
Administered IV
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Progression Free Survival (PFS)
Timepoint [1] 0 0
Baseline to Objective Progression or Death Due to Any Cause (Estimated up to 12 Months)
Secondary outcome [1] 0 0
Overall Response Rate (ORR): Percentage of Participants Who Achieve Complete Response (CR) or Partial Response (PR)
Timepoint [1] 0 0
Baseline through Measured Progressive Disease (Estimated up to 12 Months)
Secondary outcome [2] 0 0
Duration of Response (DoR)
Timepoint [2] 0 0
Date of CR or PR to Date of Objective Disease Progression or Death Due to Any Cause (Estimated up to 12 Months)
Secondary outcome [3] 0 0
Complete Response (CR): Percentage of Participants Who Achieve CR
Timepoint [3] 0 0
Baseline to date of CR (Estimated up to 12 Months)
Secondary outcome [4] 0 0
Pharmacokinetics (PK): Maximum Concentration (Cmax)
Timepoint [4] 0 0
Cycle 1 through Cycle 10 (28 Day Cycles)
Secondary outcome [5] 0 0
PK: Minimum Concentration (Cmin)
Timepoint [5] 0 0
Cycle 1 through Cycle 10 (28 Day Cycles)
Secondary outcome [6] 0 0
Number of Participants with Anti-Ramucirumab Antibodies
Timepoint [6] 0 0
Baseline through End of Study (Estimated up to 12 Months)

Eligibility
Key inclusion criteria
* Participants must have discontinued all previous treatments for cancer or investigational agents =7 days after the last dose or per the type of previous treatment as stated in the protocol and must have recovered from the acute effects to =Grade 2 for alopecia and decreased tendon reflex and to =Grade 1 for all other effects at the time of enrollment, unless otherwise noted. Consult with the Lilly clinical research physician or scientist for the appropriate length of time prior to the first dose of study treatment.
* Participants with relapsed, recurrent, or refractory DSRCT.
* Participants must:

* Have measurable disease by Response Evaluation Criteria in Solid Tumors, Version (RECIST) 1.1.
* Have received at least one prior line of systemic treatment (including neoadjuvant and adjuvant chemotherapy). This prior treatment must include approved therapies for which they are eligible, unless the participant is not a suitable candidate for the approved therapy.
* Not be eligible for surgical resection at time of enrollment.
* Adequate cardiac function, defined as: Shortening fraction of =27% by echocardiogram, or ejection fraction of =50% by gated radionuclide study.
* Adequate blood pressure (BP) control, defined as:

* Participants =18 years: Controlled hypertension defined as systolic BP =150 millimeters of mercury (mmHg) or diastolic BP =90 mmHg where standard medical management is permitted. Please note that =2 serial BP readings should be obtained and averaged to determine baseline BP.
* Participants <18 years: A BP =95th percentile for age, height, and gender measured as described in National High Blood Pressure Education Program Working Group (NHBPEPWG) on High Blood Pressure in Children and Adolescents (2004), where standard medical management is permitted. Please note that =2 serial BP readings should be obtained and averaged to determine baseline BP.
* Adequate hematologic function, as defined as:

* Absolute neutrophil count (ANC): =750/microliters (µL) granulocyte-colony stimulating factor (G-CSF) permitted up to 48 hours prior. Participants with documented history of benign ethnic neutropenia or other conditions could be considered with a lower ANC after discussion with and approval from the Lilly clinical research physician or scientist.
* Platelets: =75,000/cubic millimeters. Platelet transfusion permitted up to 72 hours prior.
* Hemoglobin: =8 grams per deciliter (g/dL) (=80 g/liter). Transfusions to increase the participant's hemoglobin level to at least 8 g/dL are permitted; however, study treatment must not begin until 7 days after the transfusion, and complete blood count criteria for eligibility are confirmed within 24 hr of first study dose.
* Adequate renal function, as defined as:

* Creatinine clearance or radioscope glomerular filtration rate (GFR) =60 milliliters/minute/meters squared OR serum creatinine meeting the following parameters:

* for participants =18 years of age serum creatinine =1.5×upper limit of normal (ULN);
* for participants <18 years of age, serum creatinine based on age/gender as follows: Age 1 to <2 years maximum serum creatinine 0.6, Age 2 to <6 years maximum serum creatinine 0.8, Age 6 to <10 years maximum serum creatinine 1.0, Age 10 to <13 years maximum serum creatinine 1.2, Age 13 to <16 years maximum serum creatinine 1.5 for males and 1.4 for females, Age 16 to <18 years maximum serum creatinine 1.7 for males and 1.4 for females.
* Urine protein meeting the following parameters:

* for participants =18 years of age: <2+ on dipstick or routine urinalysis. If urine dipstick or routine analysis indicates proteinuria =2+, then a 24-hour urine must be collected and must demonstrate <2 grams of protein in 24 hours to allow participation in the study.
* for participants <18 years of age: =30 milligrams per deciliter urine analysis or <2+ on dipstick. If urine dipstick or routine analysis indicates proteinuria =2+, then a 24-hour urine must be collected and must demonstrate <1 g of protein in 24 hours to allow participation in the study.
* Adequate liver function:

* Total bilirubin: =1.5×ULN. Except participants with document history of Gilbert Syndrome who must have a total bilirubin level of <3.0×ULN.
* Alanine aminotransferase (ALT) and aspartate aminotransferase (AST): =2.5×ULN OR =5.0×ULN if the liver has tumor involvement.
* The participant has an adequate coagulation function as defined by International Normalized Ratio =1.5 or prothrombin time =1.5×ULN, and partial thromboplastin time =1.5×ULN if not receiving anticoagulation therapy. For participants receiving anticoagulants, exceptions to these coagulation parameters are allowed if they are within the intended or expected range for their therapeutic use. Participants must have no history of clinically significant active bleeding (defined as within 14 days of first dose of study drug) or pathological condition that carries a high risk of bleeding (for example, tumor involving major vessels or known esophageal varices).
* The participant has adequate hematologic and organ function =1 week (7 days) prior to first dose of study drug.
* Female participants of childbearing potential must have a negative urine or serum pregnancy test within 7 days prior to randomization. Male and female participants must agree to use highly effective contraception for the duration of the study and up to 3 months following the last dose of ramucirumab and vinorelbine, and 12 months following the last dose of cyclophosphamide in order to prevent pregnancy.
Minimum age
12 Months
Maximum age
29 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* Participants with severe and/or uncontrolled concurrent medical disease or psychiatric illness/social situation that in the opinion of the investigator could cause unacceptable safety risks or compromise compliance with the protocol.
* Participants who have active infections requiring therapy.

* Participants with an active fungal, bacterial, and/or known severe viral infection including, but not limited to, human immunodeficiency virus (HIV) or viral (A, B, or C) hepatitis (screening is not required).
* Participants who have had allogeneic bone marrow or solid organ transplant are excluded.
* Surgery: Participants who have had, or are planning to have, the following invasive procedures are not eligible:

* Major surgical procedure, laparoscopic procedure, or significant traumatic injury within 28 days prior to enrollment.
* Central line placement or subcutaneous port placement is not considered major surgery.
* Core biopsy, fine needle aspirate, and bone marrow biopsy/aspirate are not considered major surgeries.
* Surgical or other wounds must be adequately healed prior to enrollment.
* Bleeding and thrombosis:

* Participants with evidence of active bleeding or a history of significant (=Grade 3) bleeding event within 3 months prior to enrollment are not eligible.
* Participants with a bleeding diathesis or vasculitis are not eligible.
* Participants with known or prior history in the prior 3 months of esophageal varices are not eligible.
* Participants with a history of deep vein thrombosis requiring medical intervention (including pulmonary embolism) within 3 months prior to study enrollment are not eligible.
* Participants with a history of hemoptysis or other signs of pulmonary hemorrhage within 3 months prior to study enrollment are not eligible.
* Cardiac:

* Participants with a history of central nervous system (CNS) arterial/venous thromboembolic events (VTEs) including transient ischemic attack (TIA) or cerebrovascular accident (CVA) within 6 months prior to study enrollment are not eligible.
* Participants with myocardial infarction or unstable angina within the prior 6 months.
* Participants with New York Heart Association Grade 2 or greater congestive heart failure (CHF).
* Participants with serious and inadequately controlled cardiac arrhythmia.
* Participants with significant vascular disease (eg, aortic aneurysm, history of aortic dissection).
* Participants with clinically significant peripheral vascular disease.
* Participants who have a history of fistula, gastrointestinal (GI) ulcer or perforation, or intra-abdominal abscess within 3 months of study enrollment are not eligible.
* Participants with a history of hypertensive crisis or hypertensive encephalopathy within 6 months of study enrollment are not eligible.
* Participants who have non-healing wound, unhealed or incompletely healed fracture, or a compound (open) bone fracture at the time of enrollment are not eligible.
* Participants previously treated and progressed on combination cyclophosphamide and vinorelbine regimen. Participants who received combination as maintenance therapy, without progression, would be eligible.
* Participants with a known hypersensitivity to ramucirumab, cyclophosphamide, vinorelbine or any of the excipients of the medicinal products.
* Hepatic impairment:

* Severe liver cirrhosis Child-Pugh Class B (or worse).
* Cirrhosis with a history of hepatic encephalopathy.
* Clinically meaningful ascites resulting from cirrhosis and requiring ongoing treatment with diuretics and/or paracentesis.
* History of hepatorenal syndrome.
* The participant has a bowel obstruction, history or presence of inflammatory enteropathy or extensive intestinal resection (eg, hemicolectomy or extensive small intestine resection with chronic diarrhea), Crohn's disease, ulcerative colitis, or chronic diarrhea.
* The participant has a urinary outflow obstruction.
* The participant has Grade 2 hematuria or non-infectious cystitis at the time of screening.
* Participants with central nervous system (CNS) involvement are ineligible.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Phase 1
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Active, not recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
22/01/2020
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
31/10/2024
Actual
Sample size
Target
34
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 0 0
Royal Children's Hospital - Parkville
Recruitment postcode(s) [1] 0 0
3052 - Parkville
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Arizona
Country [2] 0 0
United States of America
State/province [2] 0 0
California
Country [3] 0 0
United States of America
State/province [3] 0 0
District of Columbia
Country [4] 0 0
United States of America
State/province [4] 0 0
Missouri
Country [5] 0 0
United States of America
State/province [5] 0 0
New York
Country [6] 0 0
United States of America
State/province [6] 0 0
Oregon
Country [7] 0 0
United States of America
State/province [7] 0 0
Pennsylvania
Country [8] 0 0
Germany
State/province [8] 0 0
Baden-Württemberg
Country [9] 0 0
Germany
State/province [9] 0 0
Nordrhein-Westfalen
Country [10] 0 0
Germany
State/province [10] 0 0
Hamburg
Country [11] 0 0
Italy
State/province [11] 0 0
Lombardia
Country [12] 0 0
Italy
State/province [12] 0 0
Milano
Country [13] 0 0
Italy
State/province [13] 0 0
Roma
Country [14] 0 0
Italy
State/province [14] 0 0
Veneto
Country [15] 0 0
Japan
State/province [15] 0 0
Tokyo
Country [16] 0 0
Japan
State/province [16] 0 0
Fukuoka
Country [17] 0 0
Spain
State/province [17] 0 0
Barcelona [Barcelona]
Country [18] 0 0
Spain
State/province [18] 0 0
Sevilla
Country [19] 0 0
United Kingdom
State/province [19] 0 0
London, City Of
Country [20] 0 0
United Kingdom
State/province [20] 0 0
Sutton
Country [21] 0 0
United Kingdom
State/province [21] 0 0
Manchester

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Eli Lilly and Company
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)
Address 0 0
Eli Lilly and Company
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
What data in particular will be shared?
Anonymized individual patient level data will be provided in a secure access environment upon approval of a research proposal and a signed data sharing agreement.

Supporting document/s available: Study protocol, Statistical analysis plan (SAP), Clinical study report (CSR)
When will data be available (start and end dates)?
Data are available 6 months after the primary publication and approval of the indication studied in the US and EU, whichever is later. Data will be indefinitely available for requesting.
Available to whom?
A research proposal must be approved by an independent review panel and researchers must sign a data sharing agreement.
Available for what types of analyses?
How or where can data be obtained?
IPD available at link: http://vivli.org/


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.


Results not provided in https://clinicaltrials.gov/study/NCT04145349