Thermo Fisher's Oncomine Dx Test Is First FDA Approved NGS-Based Companion Diagnostic To Detect Thyroid Cancers


27% profit every 20 days?

This is what Nic Chahine averages with his option buys. Not selling covered calls or spreads… BUYING options. Most traders don’t even have a winning percentage of 27% buying options. He has an 83% win rate. Here’s how he does it.


  • The FDA approved Thermo Fisher Scientific Inc's (NYSE:TMO) Oncomine Dx Target Test as a companion diagnostic (CDx) to select patients with RET-fusion positive locally advanced or metastatic non-small cell lung cancer (NSCLC) and thyroid cancer who may be eligible for Eli Lilly And Co's (NYSE:LLY) Retevmo (selpercatinib) treatment.
  • Related: FDA Approves Lilly's Retevmo, the First and Only RET Inhibitor For Solid Tumor Indications.
  • This marks the Oncomine Dx Target Test's first approval as a CDx for a therapy targeting RET-positive thyroid cancer and the second approval associated with RET-positive NSCLC.
  • The Oncomine Dx Target test is a next-generation sequencing-based test that can detect multiple alterations at once from a small sample size.
  • The test is the only globally distributable NGS CDx solution that has received regulatory approval in 17 countries for 15 targeted therapies, covering more than 550 million lives globally.
  • Price Action: TMO shares closed lower by 1.10% at $508.66 on Tuesday.

27% profit every 20 days?

This is what Nic Chahine averages with his option buys. Not selling covered calls or spreads… BUYING options. Most traders don’t even have a winning percentage of 27% buying options. He has an 83% win rate. Here’s how he does it.


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