| Hint | Answer | % Correct |
|---|---|---|
| Targets HER2+ to prevent homodimerisation | trastuzumab | 63%
|
| VEGF inhibitor, restricting angiogenesis | bevacizumab | 50%
|
| CDK inhibitor for HER2- and HR+ breast cancer | palbociclib | 38%
|
| PD-L1R inhibitor for triple - breast cancer | pembrolizumab | 38%
|
| mTOR inhibitor for renal and pancreatic cancers | everolimus | 25%
|
| CDK inhibitor for HER2- and HR+ breast cancer | ribociclib | 25%
|
| Locks KRAS G12C in inactive form for NSCL cancer | adagrasib | 13%
|
| ADC for HER2+ breast cancer | ado-trastuzumab emtansine | 13%
|
| Tri-specific for EpCAM+ cancers | catumaxomab | 13%
|
| EGFR and HER1 inhibitor for bowel, neck, and head cancers | cetuximab | 13%
|
| PD-L1 inhibitor for non-small cell lung cancer (NSCL) | durvalumab | 13%
|
| PI3K inhibitor for blood cancers | idelalisib | 13%
|
| Targets HER2+ to prevent heterodimerisation with HER3 | pertuzumab | 13%
|
| Recruit E3 ligase to KRAS for degradation by ubiquitin | PROTACs | 13%
|
| G12C mutation inhibitor for NSCL cancer | sotorasib | 13%
|
| PI3K inhibitor for breast cancers | alpelisib | 0%
|
| BiTE for CD19+ ALL cancers | blinatumomab | 0%
|
| Akt inhibitor for breast cancer | capivaseritib | 0%
|
| ADC for acute lymphoblastic leukaemia (ALL) | inotuzumab ozogamicin | 0%
|
| Dual PI3K and mTOR inhibitor | paxalisib | 0%
|
| BiTE for Muc17+ cancers | vepsitamab | 0%
|