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The primary objective of this combination treatment was to improve local tumor control.
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The primary objective of this phase I combination trial was to determine the dose-limiting toxicities (DLTs) and RP2D of aflibercept administered i.v. every 3 weeks in combination with pemetrexed and cisplatin.
The primary objective of this study was to estimate the MTD and RD of the combination therapy including weekly nab-paclitaxel and S-1 in patients with MBC.
The primary objective of this study was to determine the MTD for the combination regimen of vorinostat, lenalidomide and dexamethasone in patients with relapsed or refractory MM.
The primary objective of this study was to identify the recommended dose of the combination of sorafenib and sirolimus for subsequent phase II studies.
The primary objective of this phase II study was to determine the efficacy of a combination of gemcitabine and raltitrexed in advanced or metastatic adenocarcinoma of the pancreas.
The primary objective of this study was to establish the optimal dose of cyclophosphamide in combination with fixed doses of bortezomib and dexamethasone.
The primary objective of this review was to assess the antiviral efficacy of abacavir-containing combination antiretroviral therapy (cART) regimens in comparison with cART regimens containing other NRTIs as first-line therapy for HIV infected children and adolescents.
The primary objective of this study was to determine the antitumor activity of Imprime PGG in combination with cetuximab in patients with KRAS-mutant metastatic CRC.
The primary objective of this study was to determine the MTD of HCQ when given in combination with dose intense TMZ in patients with refractory solid tumors.
The primary objective of this study was to determine the safety and tolerability of MuStDO5 in combination with escalating dose hGM-CSF plasmid in healthy, malaria-naïve, adult volunteers.
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