Safety Study of an Immune Response Modifier in Patients With Refractory Solid Organ Tumors

Mise à jour : Il y a 4 ans
Référence : NCT00095160

Femme et Homme

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Extrait

Study 1493-852A is a phase 1 study with the primary objective of determining safety and the highest tolerated dose of an experimental immune response modifier administered intravenously to patients with solid organ tumors not responsive to currently available treatments. The secondary objective of the study is to monitor the tumor response to this form of treatment.


Critère d'inclusion

  • Neoplasms

Liens