Compassionate Use Antiangiogenic Therapy in Dogs with Measurable Malignant Melanomas or Myelomas
Eligibility:
* Owner informed consent
* Client owned pet dogs
* Histologically confirmed malignant melanoma or myeloma
* Tumors must be objectively measurable using direct caliper measurement (documented by digital image and investigator documentation on evaluation form), ultrasound, radio-graphs or CT/MRI scan.
* Favorable clinical performance status at entry (expected to remain clinically stable for 30 days)
* No previous exposure to antiangiogenic therapies
* No chemotherapy within 14 days of trial entry
* No radiation therapy administered within 21 days of trial entry
* Corticosteroids and non-steroidal anti-inflammatory agents ok to continue if patient has been receiving for >14 days at time of study entry
Trial Support:
Antiangiogenic peptide will be provided at no charge. All examination, tumor imaging and other diagnostic costs are the patient”s responsibility, including a $50 monthly service fee ($50, billable to the Network clinic/investigator). All patients must be evaluated and treated monthly through a participating Animal Cancer Institute Network site. Diagnostic and staging tests may be performed at any veterinary hospital within 10 days of initiation (full serum chemistry, CBC, U/A and thoracic radiographs). Dogs will receive a month”s supply of medication for in-home, daily subcutaneous injection. Continued therapy will be available pending response to therapy.









Pet owners seeking novel treatment options for animals with serious health conditions find an Animal Clinical Investigation network veterinarian participating in a clinical trial.
Animal Clinical Investigation network veterinarian and pet owner work together to determine whether the pet is eligible for the trial. Eligible pets begin treatment at an ACI network hospital.
Information from the trial is used to help develop new drugs and treatments, providing a source of hope for people whose pets face serious illnesses.