Literature DB >> 9073527

Safety evaluation of recombinant human interleukin-4. II. Clinical studies.

M W Leach1, M E Rybak, I Y Rosenblum.   

Abstract

The safety and tolerability of Escherichia coli-derived recombinant human interleukin-4 (rhuIL-4) have been evaluated in phase I and phase II studies in human patients with a variety of malignancies. Clinical trials have demonstrated that subcutaneous administration of rhuIL-4 is safe and well tolerated at doses as high as 5 micrograms/kg/day and as high as 10 micrograms/kg when administered 3 times/week. Although preclinical safety studies in cynomolgus monkeys demonstrated a number of adverse effects following repeated daily dosing with rhuIL-4, similar effects have generally not been observed in human patients.

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Year:  1997        PMID: 9073527     DOI: 10.1006/clin.1997.4304

Source DB:  PubMed          Journal:  Clin Immunol Immunopathol        ISSN: 0090-1229


  2 in total

1.  Phase II study of interleukin-4 in indolent B-cell non-Hodgkin lymphoma and B-cell chronic lymphocytic leukemia: a study of the Eastern Cooperative Oncology Group (E5Y92).

Authors:  Peter H Wiernik; Janice P Dutcher; Xiapan Yao; Usha Venkatraj; Carla I Falkson; Jacob M Rowe; Peter A Cassileth
Journal:  J Immunother       Date:  2010 Nov-Dec       Impact factor: 4.456

2.  Targeted cancer gene therapy using a hypoxia inducible factor dependent oncolytic adenovirus armed with interleukin-4.

Authors:  Dawn E Post; Eric M Sandberg; Michele M Kyle; Narra Sarojini Devi; Daniel J Brat; Zhiheng Xu; Mourad Tighiouart; Erwin G Van Meir
Journal:  Cancer Res       Date:  2007-07-15       Impact factor: 12.701

  2 in total

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