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{|border="2" cellspacing="0" cellpadding="4" width="100%"
|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''S.No.'''</font>
|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''Drug Name'''</font>
|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''Biological Name'''</font>
|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''Developer'''</font>
|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''Current Development Phase'''</font>
|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''Additional Information'''</font>
|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''Start Date'''</font>
|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''Completion Date'''</font>
|bgcolor = "#4F81BD"|<font color="#FFFFFF">'''Source'''</font>
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|align = "center" bgcolor = "#DBE5F1"|11
|bgcolor = "#DBE5F1"|E7-specific cancer vaccines
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|bgcolor = "#DBE5F1"|National Taiwan University Hospital
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|bgcolor = "#DBE5F1"|There are two main goals in this study. First, the investigators would like to establish and compare the differences of HPV type 16 E7-specific immunologic responses between the normal population, people with HPV infection, patients with cervical intraepithelial neoplastic (CIN) lesions, and patients with cervical cancer. Second, they would like to correlate the disease severity of cervical cancer with the immunologic responses to HPV type 16 E7 antigen
|bgcolor = "#DBE5F1"|2003
|bgcolor = "#DBE5F1"|2008
|bgcolor = "#DBE5F1"|<font color="#0000FF"><u>[http://clinicaltrials.gov/ct2/show/NCT00154583?term=cancer+vaccine&rank=29 Source]</u></font>
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|RG3484
|Roche
|II
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|bgcolor = "#DBE5F1"|Therapeutic<br>Vaccine
|bgcolor = "#DBE5F1"|Transgene
|bgcolor = "#DBE5F1"|Preclinical
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