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1 been shown to be as effective as intravenous pamidronate.
2 renal function before the administration of pamidronate.
3 site in men treated with both leuprolide and pamidronate.
4 ng thalidomide (THAL, 200 mg/d) with monthly pamidronate.
5 in cultures treated with the bisphosphonate pamidronate.
6 also increased in osteoblasts cultured with pamidronate.
7 controlled, randomized, nonblinded trial of pamidronate (30 mg intravenously every 3 mo) with vitami
9 ults of two randomized trials that evaluated pamidronate 90 mg administered intravenously every month
11 ession fracture from osteopenia, intravenous pamidronate 90 mg delivered over at least 2 hours or zol
12 mg subcutaneously every 4 weeks, intravenous pamidronate 90 mg over no less than 2 hours, or zoledron
13 one lytic lesion received either placebo or pamidronate (90 mg) as a four-hour intravenous infusion
14 tic bone lesion were given either placebo or pamidronate (90 mg) as a two-hour intravenous infusion m
15 sumab, 120 mg subcutaneously, every 4 weeks; pamidronate, 90 mg intravenously, every 3 to 4 weeks; or
16 is directly, we injected postnatal rats with pamidronate, a bisphosphonate that reduces bone resorpti
17 of infected, reconstituted hu-SCID mice with pamidronate, a human V gamma 2V delta 2 T cell-specific
18 dy that treatment of murine macrophages with pamidronate, a second generation aminobisphosphonate, in
20 2H NMR measurements of side-chain 2H-labeled pamidronate, alendronate, zoledronate, and risedronate o
24 One hundred eighty-two patients who received pamidronate and 189 who received placebo were assessable
27 oxyalkyl, and sulfanylalkyl) derivatives of pamidronate and one alendronate, a molecular field analy
29 ustained significant differences between the pamidronate and placebo groups in self-reported pain mea
33 ng free divalent ion concentrations, whereas pamidronate and zoledronate appear to act on the hFOB ce
37 ed treatment with the potent bisphosphonates pamidronate and zoledronic acid seems to be well tolerat
39 t supports that oral clodronate, intravenous pamidronate, and intravenous zoledronic acid are superio
40 decreased with monthly infusions of 90 mg of pamidronate, and this effect was maintained for at least
42 sphosphonates, particularly the potent agent pamidronate (Aredia), will relieve metastatic bone pain
50 ore, pretreatment of murine macrophages with pamidronate before stimulation with IFN-gamma significan
56 the effect of an intravenous bisphosphonate, pamidronate disodium, on pain control in metastatic pros
57 s were treated with docetaxel, docetaxel and pamidronate disodium, or docetaxel and cyclophosphamide.
62 hat clinicians consider reducing the initial pamidronate dose in patients with pre-existing renal imp
63 ed 9 or more doses of zoledronic acid and/or pamidronate during the first 10 to 15 months of therapy.
64 ned the effects of alendronate, risedronate, pamidronate, etidronate, and clodronate on apoptosis and
68 eletal events was significantly lower in the pamidronate group (24 percent) than in the placebo group
69 had any skeletal complication was 56% in the pamidronate group and 67% in the placebo group (P = .027
71 rst skeletal complication was greater in the pamidronate group than in the placebo group (13.1 vs. 7.
73 of skeletal events per year was less in the pamidronate-group (1.3) than in placebo-treated patients
78 ogen-containing bisphosphonates alendronate, pamidronate, homorisedronate, and risedronate but was le
79 nsplantation, all patients received 90 mg of pamidronate i.v. every 12 weeks, regardless of pretransp
82 trial was conducted using the bisphosphonate pamidronate intravenously in patients with new renal tra
84 riments indicate that the NH3(+)-terminus of pamidronate is close to the bone mineral surface, and a
89 nts overall, stratum 2 patients who received pamidronate lived longer than those who received placebo
92 e an approximately 30-38 A2 surface area per pamidronate molecule and a deltaG = -4.3 kcal mol(-1).
93 ate therapy included zoledronate (n = 34) or pamidronate (n = 17) and pamidronate followed by zoledro
96 onate, were also compared with the action of pamidronate on proliferation of immortalized human fetal
97 hylamino)ethyl diphosphate, alendronate, and pamidronate on the pools of metabolites related to monot
98 therapy were randomized to receive 90 mg of pamidronate or placebo as a 2-hour intravenous infusion
99 randomly assigned to receive either 90 mg of pamidronate or placebo intravenously every 3 to 4 weeks
100 vations strongly suggest that treatment with pamidronate or zoledronate enhances the differentiation
101 reatment of PC3, DU145, and LNCaP cells with pamidronate or zoledronate significantly reduced the gro
102 studied 22 patients who received intravenous pamidronate or zoledronic acid for a duration of 3.6 yea
103 wever, the panel recommends only intravenous pamidronate or zoledronic acid in light of the use of th
105 no direct comparisons between clodronate and pamidronate or zoledronic acid, the superiority of one a
106 24 cycles in patients treated with 90 mg of pamidronate (P = .028, .023, and .008, respectively).
107 orubicin (Doxo) and coated with bone-seeking pamidronate (Pam) for the targeted treatment of malignan
108 Intravenous (IV) zoledronic acid (ZOL) or pamidronate (PAM) is recommended for preventing skeletal
109 ral mucosal tissue, we studied the effect of pamidronate (PAM), one of the BPs most commonly administ
116 n vivo (potency: risedronate > alendronate > pamidronate) requires expression of the Vgamma2Vdelta2 T
117 mplication was longer for patients receiving pamidronate than for those given placebo (P = .049).
118 complication was significantly less for the pamidronate than the placebo group at 15, 18, 21, and 24
121 similar dosing guidelines are available for pamidronate, the Update Committee recommends that clinic
124 hough survival was not different between the pamidronate-treated group and placebo patients overall,
125 skeletal complication was 13.9 months in the pamidronate-treated women and 7.0 months in the placebo
131 e effects in vivo of the bisphosphonate drug pamidronate, used in bone resorption therapy, were inves
132 -hoc evaluation of the cost-effectiveness of pamidronate using the results of two randomized trials t
139 rseded by second-generation bisphosphonates (pamidronate), which are more potent and do not have adve
142 15 minutes), versus the less expensive drug, pamidronate, with its longer infusion time (2 hours).
143 dental extraction (P = .009), treatment with pamidronate/zoledronate (P = .009), longer follow-up tim
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