Ȩ |  ÁÖ¿ä ÇÁ·Î±×·¥ |  ½ÉÆ÷Áö¾ö |  ÆÄÆ®³Ê¸µ Æ÷·³ |  ¿¬»ç ¾È³» |  ¼îÆ®ÄÚ½º |  ½ºÆù¼­ |  Æ÷½ºÅÍ Á¤º¸ |  °³ÃÖÁö |  ºê·Î¼Å(PDF) | ¹®ÀÇ |  Âü°¡½Åû |  (ÁÖ)±Û·Î¹úÀÎÆ÷¸ÞÀ̼Ç

Call for Speaker Proposals

Á¦2ȸ
Oncology Clinical Trials
-¾ÏÄ¡·áÁ¦ ÀÓ»ó½ÃÇè ÇÐȸ-

ÀÓ»ó½ÃÇèÀÇ °³¼±¿¡ ÀÇÇÑ ¾ÏÄ¡·áÁ¦ °³¹ßÀÇ ÃËÁø
2¿ù 21ÀÏ¡­23ÀÏ

ÃÖ±Ù ¾ÏºÐÀÚ»ý¹°ÇÐ ¿¬±¸ÀÇ ´«ºÎ½Å ¼º°ú·Î ÀÎÇØ ¾ÏÄ¡·áÁ¦ °³¹ß ºÐ¾ß¿¡¼­´Â Àü·Ê¾øÀÌ ¸¹Àº »õ·Î¿î Ç¥ÀûÀÌ »ý¼ºµÇ°í ÀÖ½À´Ï´Ù. ÀÌ¿Í °°Àº Ç¥Àû ´ë»ó ¾àÁ¦ÀÇ ´Ù ¼ö´Â ÀÌ¹Ì ÀÓ»ó ´Ü°è·Î ÁøÇàµÇ°í ÀÖÀ¸¸ç, ´Ù¾çÇÑ Ä¡·á¹ýÀ» À§ÇÑ ¾ÏÄ¡·áÁ¦ÀÇ ÀÓ»ó½ÃÇèÀÌ È°¹ßÈ÷ ÁøÇàµÇ°í ÀÖ½À´Ï´Ù. ¾ÏÄ¡·áÁ¦ÀÇ ÀÓ»ó½ÃÇèÀ» ¼º°ø½Ã۱â À§ÇÑ ¿äÀÎÀº ¸¹ÀÌ ÀÖÀ¸³ª, °¡Àå Áß¿äÇÑ ¿äÀÎÀº ÀÓ»óÀü µ¥ÀÌÅͰ¡ °ËÁõ°¡´ÉÇÑ °¡¼³À» µµÃâÇÏ´Â °ÍÀÌ °¡´ÉÇÑ ¼öÁØ¿¡ µµ´ÞÇߴ°¡¶ó´Â Á¡ÀÔ´Ï´Ù. ¶ÇÇÑ »ý¹°Åë°èÇÐ, °ú ÇÐ, Á¶Á÷, ±ÔÁ¦, À±¸®, °æÁ¦ µî¿¡ °ü·ÃµÈ ¿äÀεµ ÀǾàǰÀÇ ÀÓ»ó°³¹ßÀ» ÁøÇà½Ã۴µ¥ Áß¿äÇÑ Àǹ̸¦ Áö´Ï°í ÀÖ½À´Ï´Ù.

Who should attend: Scientists, biostatisticians, project managers, research investigators and other specialists involved in oncology clinical trials

Topics will include, but are not limited to:

  • Translational clinical trials in oncology
  • Evaluating pre-clinical evidence to avoid clinical development failures
  • Molecular imaging in cancer clinical trials
  • Prescreening patients for somatic mutations before randomization
  • Biomarker-driven clinical trials
  • Companion diagnostics in oncology clinical trials
  • Advanced methodology for dose-finding clinical trials
  • Dose finding for ¡°nontoxic¡± drug
  • Pharmacodynamic biomarkers and their use in clinical trials
  • Role of randomization in middle development
  • How to use surrogate outcomes in the light of lack of biomarker validation
  • Regulatory and legal challenges and solutions
  • Safety issues in cancer clinical trials
  • Ways to increase patient enrollment
  • Ethical issues related to biomarker use for patient selection (what is the threshold?)
  • Cost effectiveness of clinical trials in the US and abroad
  • Joint development: Industry-academic collaboration (identification (who takes responsibility), shared intellectual property, etc.)

The deadline for submission is July 29, 2011.

All proposals are subject to review by the Scientific Advisory Committee to ensure the highest quality of the conference program. Please note that due to limited speaking slots, preference is given to pharmaceutical and biotech companies, regulators and those from academia. Additionally, vendors/consultants who provide products and services to these biopharmaceutical companies are
offered opportunities for podium presentation slots based on a variety of Corporate Sponsorships.


Choose your language
English
Japan
Traditional Chinese
Simplified Chinese

À̺¥Æ® ͏°´õ
¹ÙÀÌ¿ÀÅ×Å©³î·¯Áö °ü·Ã ±¹Á¦ÄÁÆÛ·±½º

¹ÙÀÌ¿ÀÅ×Å©³î·¯Áö °ü·Ã ±¹Á¦ÄÁÆÛ·±½º