Pulmonary fibrosis is scarring of the lungs that can arise from radiation injury, drug toxicity, environmental or genetic causes, and for unknown reasons [idiopathic pulmonary fibrosis (IPF)]. Overexpression of collagen is a hallmark of organ fibrosis. We describe a peptide-based positron emission tomography (PET) probe (⁶⁸Ga-CBP8) that targets collagen type I. We evaluated ⁶⁸Ga-CBP8 in vivo in the bleomycin-induced mouse model of pulmonary fibrosis. ⁶⁸Ga-CBP8 showed high specificity for pulmonary fibrosis and high target/background ratios in diseased animals. The lung PET signal and lung ⁶⁸Ga-CBP8 uptake (quantified ex vivo) correlated linearly (r² = 0.80) with the amount of lung collagen in mice with fibrosis. We further demonstrated that the ⁶⁸Ga-CBP8 probe could be used to monitor response to treatment in a second mouse model of pulmonary fibrosis associated with vascular leak. Ex vivo analysis of lung tissue from patients with IPF supported the animal findings. These studies indicate that ⁶⁸Ga-CBP8 is a promising candidate for noninvasive imaging of human pulmonary fibrosis.