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1.
Fig. 3.

Fig. 3. From: A phase I clinical trial with monoclonal antibody ch806 targeting transitional state and mutant epidermal growth factor receptors.

Individual patient results for normalized whole body clearance (A) and hepatic clearance (B) of 111In-ch806 at the 5 mg/m2 (■), 10 mg/m2 (▵), 20 mg/m2 (▿), and 40 mg/m2 (⧫) dose levels. Linear regression for data sets is indicated in each image [r2 = 0.9595 (A); r2 = 0.9415 (B)].

Andrew M. Scott, et al. Proc Natl Acad Sci U S A. 2007 Mar 6;104(10):4071-4076.
2.
Fig. 1.

Fig. 1. From: A phase I clinical trial with monoclonal antibody ch806 targeting transitional state and mutant epidermal growth factor receptors.

Biodistribution and tumor localization of 111In-ch806. (A and B) Whole body gamma camera images of patient 7, anterior (A) and posterior (B), on day 5 after infusion of 111In-ch806. High uptake of 111In-ch806 in metastatic lesions in the lungs (arrows) is evident. (C and D) Metastatic lesions (arrows) on scan. (E) 3D SPECT images of the chest. (F) Coregistered transaxial images of SPECT and CT showing specific uptake of 111In-ch806 in metastatic lesions.

Andrew M. Scott, et al. Proc Natl Acad Sci U S A. 2007 Mar 6;104(10):4071-4076.
3.
Fig. 2.

Fig. 2. From: A phase I clinical trial with monoclonal antibody ch806 targeting transitional state and mutant epidermal growth factor receptors.

ch806 targeting of glioma. (AC) Planar images of the head and neck of patient 8 obtained on day 0 (A), day 3 (B), and day 7 (C) after infusion of 111In-ch806. Initial blood pool activity is seen on day 0, and uptake of 111In-ch806 in an anaplastic astrocytoma in the right frontal lobe is evident by day 3 (arrow) and increases by day 7. (DF) Specific uptake of 111In-ch806 is confirmed in SPECT image of the brain (D) (arrow), at the site of tumor (arrow) evident in 18F-FDG (FDG, Fluorodeoxyglucose) positron emission tomography (E), and MRI (F).

Andrew M. Scott, et al. Proc Natl Acad Sci U S A. 2007 Mar 6;104(10):4071-4076.

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