: The frequent overexpression of gastrin-releasing peptide receptors (GRPRs) in human cancers provides the rationale for delivering clinically useful radionuclides to tumor sites using peptide carriers. Radiolabeled GRPR antagonists, besides being safer for human use, have often shown higher tumor uptake and faster background clearance than agonists. We herein compared the biological profiles of the GRPR-antagonist-based radiotracers TcTc-N -PEGx-DPhe ,Leu-NHEt BBN(6-13) (N : 6-(carboxy)-1,4,8,11-tetraazaundecane; PEG: polyethyleneglycol): (i) TcTc-DB7 (x = 2), (ii) TcTc-DB13 (x = 3), and (iii) TcTc-DB14 (x = 4), in GRPR-positive cells and animal models. The impact of in situ neprilysin (NEP)-inhibition on in vivo stability and tumor uptake was also assessed by treatment of mice with phosphoramidon (PA). : The GRPR affinity of DB7/DB13/DB14 was determined in PC-3 cell membranes, and cell binding of the respective TcTc-radioligands was assessed in PC-3 cells. Each of TcTc-DB7, TcTc-DB13, and TcTc-DB14 was injected into mice without or with PA coinjection and 5 min blood samples were analyzed by HPLC. Biodistribution was conducted at 4 h postinjection (pi) in severe combined immunodeficiency disease (SCID) mice bearing PC-3 xenografts without or with PA coinjection. : DB7, -13, and -14 displayed single-digit nanomolar affinities for GRPR. The uptake rates of TcTc-DB7, TcTc-DB13, and TcTc-DB14 in PC-3 cells was comparable and consistent with a radioantagonist profile. The radiotracers were found to be ≈70% intact in mouse blood and >94% intact after coinjection of PA. Treatment of mice with PA enhanced tumor uptake. : The present study showed that increase of PEG-spacer length in the TcTc-DB7- TcTc-DB13- TcTc-DB14 series had little effect on GRPR affinity, specific uptake in PC-3 cells, in vivo stability, or tumor uptake. A significant change in in vivo stability and tumor uptake was observed only after treatment of mice with PA, without compromising the favorably low background radioactivity levels.