Patients must not demonstrate any other signs indicative of pulmonary hemorrhage within  months prior to registration
The subject has experienced any of the following:\r\n* Clinically-significant GI bleeding within  months before the first dose of cabozantinib\r\n* Hemoptysis of >= . teaspoon (. ml) of red blood within  months before the first dose of cabozantinib\r\n* Any other signs indicative of pulmonary hemorrhage within  months before the first dose of cabozantinib
The subject has experienced any of the following:\r\n* Clinically-significant gastrointestinal (GI) bleeding within  months before the first dose of study treatment\r\n* Hemoptysis of >= . teaspoon (. ml) of red blood within  months before the first dose of study treatment\r\n* Any other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment
The participant has experienced any of the following:\r\n* Clinically-significant gastrointestinal bleeding within  months before the first dose of study treatment\r\n* Hemoptysis of >= . teaspoon (. mL) of red blood within  months before the first dose of study treatment\r\n* Any other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment
The subject has experienced any of the following: a. clinically-significant gastrointestinal bleeding within  months before the first dose of study treatment; b. hemoptysis >= . teaspoon (. mL) of red blood within  months before the first dose of study treatment; c. any other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment. Tumor invading any major blood vessel at the time of study enrollment.
The subject has experienced any of the following:\r\n* Clinically significant gastrointestinal bleeding within  months before the first dose of study treatment\r\n* Clinically significant hemoptysis within  months of the first dose of study treatment\r\n* Any other signs indicative of pulmonary hemorrhage within  months before the start of study treatment
The subject has any of the following risks of bleeding:\r\n* Clinically-significant gastrointestinal (GI) bleeding within  months before enrollment\r\n* Hemoptysis of >= . teaspoon (. ml) of red blood within  months enrollment\r\n* Any other signs indicative of pulmonary hemorrhage within  months before enrollment\r\n* Radiographic evidence of cavitating pulmonary lesion(s)
The subject has experienced any of the following:\r\n* Clinically-significant gastrointestinal (GI) bleeding within  months before the first dose of study treatment\r\n* Hemoptysis of >= . teaspoon (. ml) of red blood within  months before the first dose of study treatment\r\n* any other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment; and\r\n* Clinically confirmed history of interstitial lung disease (ILD)
The subject has experienced any of the following:\r\n* Clinically-significant gastrointestinal bleeding within  months before the first dose of study treatment\r\n* Hemoptysis of >= . teaspoon (. mL) of red blood within  months before the first dose of study treatment\r\n* Any other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment\r\n* The subject has radiographic evidence of cavitating pulmonary lesion(s); chest x-ray will not be required as part of this trial, unless cavitating pulmonary lesion is clinically suspected
The subject has experienced any of the following: \r\n* Clinically-significant gastrointestinal bleeding within  months before the first dose of study treatment; \r\n* Hemoptysis of >= . teaspoon (. mL) of red blood within  months before the first dose of study treatment; \r\n* Any other signs indicative of hemorrhage within  months before the first dose of study treatment
The subject has experienced any of the following:\r\n* Clinically-significant gastrointestinal bleeding within  months before the first dose of study treatment\r\n* Hemoptysis of >= . teaspoon (. mL) of red blood within  months before the first dose of study treatment\r\n* Any other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment
Clinically significant hematemesis or hemoptysis of > . teaspoon (. ml) of red blood, or other history of significant bleeding (such as pulmonary hemorrhage) within  weeks of enrollment
The subject has experienced any of the following: a. clinically-significant gastrointestinal bleeding within  months before the first dose of study treatment, b. hemoptysis of >= . teaspoon (. ml) of red blood within  months before the first dose of study treatment, c. any other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment
The subject has experienced any of the following:\r\n* Clinically-significant gastrointestinal bleeding within  months before the first dose of study treatment\r\n* Hemoptysis of >= . teaspoon (. ml) of red blood within  months before the first dose of study treatment\r\n* Any other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment
The subject has experienced any of the following:\r\n* Clinically-significant gastrointestinal bleeding within  months before the first dose of study treatment\r\n* Hemoptysis of >= . teaspoon (.ml) of red blood within  months before the first dose of study treatment\r\n* Any other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment
The subject has experienced any of the following:\r\n* Clinically-significant GI bleeding within  months before the first dose of study treatment\r\n* Hemoptysis of >= . teaspoon (. ml) of red blood within  months before the first dose of study treatment\r\n* Any other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment
The subject has experienced any of the following:\r\n* Clinically-significant gastrointestinal bleeding within  months before the first dose of study treatment\r\n* Hemoptysis of >= . teaspoon (. mL) of red blood within  months before the first dose of study treatment\r\n* Any other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment
The subject has experienced clinically-significant hematemesis or hemoptysis of > . teaspoon of red blood, or other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment
The subject has experienced any of the following within  months before the first dose of\r\nstudy treatment:\r\n* Clinically-significant hematemesis or lower gastrointestinal bleeding\r\n* Hemoptysis of > . teaspoon of red blood\r\n* Any other signs indicative of pulmonary hemorrhage
No signs indicative of pulmonary hemorrhage within  weeks before the first dose of study treatment
Previously experienced any of the following:\r\n* Clinically significant gastrointestinal bleeding within  months\r\n* Hemoptysis of >= . teaspoon (. ml) of red blood within the last  months\r\n* Any other signs indicative of pulmonary hemorrhage within  months
Previously experienced any of the following:\r\n* Clinically significant gastrointestinal bleeding within  months before the first dose of study treatment\r\n* Hemoptysis of >= . teaspoon (. ml) of red blood within  months before the first dose of study treatment\r\n* Any other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment
The subject has experienced any of the following within  months before the first dose of study treatment:\r\n* Clinically-significant hematemesis or gastrointestinal bleeding\r\n* Hemoptysis of >= . teaspoon (>= . mL) of red blood\r\n* Any other signs indicative of pulmonary hemorrhage
Patients with active bleeding or pathologic conditions that carry high risk of bleeding, such as known bleeding disorder, coagulopathy, or tumor involving (in contact with, invading or encasing) major vessels; patients who have experienced any of the following:\r\n* Clinically significant gastrointestinal bleeding within  months before first dose of study treatment\r\n* Hemoptysis of >= . teaspoon (. ml) of red blood within  months before the first dose of study treatment\r\n* Any other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment
The subject has experienced any of the following:\r\n* Clinically-significant hematemesis or gastrointestinal bleeding within  months before the first dose of study treatment\r\n* Hemoptysis of >= . teaspoon (. mL) of red blood within  months before the first dose of study treatment\r\n* Any other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment
The participant has experienced any of the following within  months before the first dose of study treatment:\r\n* Clinically-significant hematemesis or lower gastrointestinal bleeding\r\n* Hemoptysis of >= . teaspoon (. ml) of red blood\r\n* Any other signs indicative of pulmonary hemorrhage
The subject has a history of clinically significant hematemesis or a recent history of hemoptysis of > . mL of red blood or other signs indicative of pulmonary hemorrhage or evidence of endobronchial lesion(s)
The subject has experienced any of the following:\r\n* Clinically significant gastrointestinal bleeding within  months before the first dose of study treatment\r\n* Hemoptysis of >= . teaspoon (. mL) of red blood within  months before the first dose of study treatment\r\n* Any other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment
The subject has experienced any of the following:\r\n* Clinically-significant gastrointestinal bleeding within  months before the first dose of study treatment\r\n* Hemoptysis of >= . teaspoon (. mL) of red blood within  months before the first dose of study treatment\r\n* Any other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment
Subject has had clinically-significant hematemesis or hemoptysis of > . teaspoon of red blood, or other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment
The subject has experienced any of the following within  months before the first dose of study treatment:\r\n* Clinically significant hematemesis or gastrointestinal bleeding\r\n* Hemoptysis of >= . teaspoon (. ml) of red blood\r\n* Any other signs indicative of pulmonary hemorrhage
The subject has experienced any of the following\r\n* Clinically-significant gastrointestinal bleeding within  months before the first dose of study treatment; the participant must be maintained on a prophylactic regimen for management of an upper gastrointestinal (GI) bleeding event with no evidence of recurrence and/or endoscopic confirmation of resolution of the source of a lower GI bleed\r\n* Hemoptysis of >= . teaspoon (. mL) of red blood within  months before the first dose of study treatment\r\n* Any other signs indicative of pulmonary hemorrhage within  months before the first dose of study treatment
The subject has experienced any of the following within  months before the first dose of study treatment:\r\n* Clinically-significant hematemesis or gastrointestinal bleeding\r\n* Clinically-significant hemoptysis of >= . teaspoon (. ml) of red blood\r\n* Any other signs indicative of pulmonary hemorrhage