2010
DOI: 10.1016/j.ejca.2010.07.015
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Early cessation of the clinical development of LiPlaCis, a liposomal cisplatin formulation

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Cited by 79 publications
(32 citation statements)
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“…In the study, the drug was given as an i.v. infusion over one hour, every three weeks in advanced breast cancer patients (de Jonge et al 2010). Unfortunately, the study ended early as the results demonstrated no benefit in the dose or toxicity profile when compared with normal cisplatin.…”
Section: Liplacismentioning
confidence: 99%
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“…In the study, the drug was given as an i.v. infusion over one hour, every three weeks in advanced breast cancer patients (de Jonge et al 2010). Unfortunately, the study ended early as the results demonstrated no benefit in the dose or toxicity profile when compared with normal cisplatin.…”
Section: Liplacismentioning
confidence: 99%
“…Unfortunately, the study ended early as the results demonstrated no benefit in the dose or toxicity profile when compared with normal cisplatin. The study concluded that LaPlaCis needed reformulation if it was to be effective (de Jonge et al 2010).…”
Section: Liplacismentioning
confidence: 99%
“…NOVEL APPROACHES FOR CANCER THERAPIES was stopped after a Phase I study when it was found that LiPlaCis did not prevent the renal toxicity of cisplatin and the incidence of acute infusion reactions was relatively high in this trial. 26 Finally, a liposomal formulation of vinorelbine (NanoVNB ® ) 27 is in clinical development (Phase I/II trials). As we do not want to replicate the earlier reviews by Chang and Yen, 19 Sen and Mandal, 20 Slingeland et al, 21 and Koudelka and Turanek, 22 we limit our examples to these few.…”
Section: Liposomes For the Delivery Of Chemotherapeuticsmentioning
confidence: 99%
“…There are over 1000 clinical trials containing the terms "liposome" and "cancer," either completed or active, according to The National Institutes of Health's (NIH) web-based database, ClinicalTrials.gov and the EU Clinical Trial Register. There are several ongoing clinical trials investigating the efficiency of liposomal cisplatin, NDDP (cisplatin analog), paclitaxel, mitoxantrone, irinotecan, SN38 (the active metabolite of irinotecan), topotecan, lurtotecan, a camptothecin analog, vinorelbine, annamycin, docetaxel, DOX, and vincristine [83][84][85][86][87]. The association of chemotherapeutic drugs is a frequently used strategy in chemotherapy.…”
Section: Clinical Experience With Liposomes For Cancer Chemotherapymentioning
confidence: 99%