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Exelixis Announces U S FDA Approval of CABOMETYX® (cabozantinib) for Patients with Previously Treated Radioactive Iodine-Refractory Differentiated Thyroid Cancer | Small Molecules

Exelixis Announces U S FDA Approval of CABOMETYX® (cabozantinib) for Patients with Previously Treated Radioactive Iodine-Refractory Differentiated Thyroid Cancer | Small Molecules
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United statesMarcias broseDrug administrationTakeda pharmaceutical companyAmerican thyroid associationIexelixis incExelixis incEuropean thyroid association guidelines for the treatmentCommunity based clinical trialsEuropean unionAmerican cancer societyPrescription drug user fee actUnited statesi septemberBreakthrough therapyPriority reviewJefferson torresdale hospital

Opdivo (nivolumab) Plus Yervoy (ipilimumab) Demonstrates Durable Overall Survival at Three Years Compared to Chemotherapy in First-Line Unresectable Malignant Pleural Mesothelioma in Phase 3 CheckMate -743 Trial | Antibodies

Opdivo (nivolumab) Plus Yervoy (ipilimumab) Demonstrates Durable Overall Survival at Three Years Compared to Chemotherapy in First-Line Unresectable Malignant Pleural Mesothelioma in Phase 3 CheckMate -743 Trial | Antibodies
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United statesSouth koreaAbderrahim oukessouIbristol myers squibbSolange petersCompany opdivoBristol myers squibb companyOncology serviceEuropean society for medical oncology virtual congressEuropean unionLausanne university hospitalVirtual congressBristol myers squibbDrug administrationOno pharmaceutical coEuropean society for medical oncology

GT Biopharma Advances GTB-3650, a Second-Generation Tri-Specific Killer Engager -TriKE®, Into IND-Enabling Studies | Antibodies

GT Biopharma Advances GTB-3650, a Second-Generation Tri-Specific Killer Engager -TriKE®, Into IND-Enabling Studies | Antibodies
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Cytovance biologicsBeverly hillsGreg berkI gt biopharma incSecond generation tri specific killer engagerEnabling studiesUnited statesi septemberChief medicalTri specific killer engagerபெவர்லி மலைகள்கிரெக் பெர்க்செயல்படுத்துகிறது ஆய்வுகள்தலைமை மருத்துவ

Nuvectis Pharma In-Licenses Exclusive Worldwide Rights to a Novel SRC/YES1 Inhibitor (NXP900) from the University of Edinburgh, Scotland | More News

Nuvectis Pharma In-Licenses Exclusive Worldwide Rights to a Novel SRC/YES1 Inhibitor (NXP900) from the University of Edinburgh, Scotland | More News
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United kingdomCity ofNeil carragherRon bentsurNuvectis pharmaHead of the innovative therapeutics labInstitute of geneticsUniversity of edinburghCancer researchI nuvectis pharma incInstitute of cancer researchNuvectis pharma incQs world university rankingsDifferentiated mechanismUnited statesi septemberCancer research united kingdom edinburgh centre

Convergent Therapeutics and Point Biopharma Announce a Collaboration to Evaluate CONV 01-α (Rosopatamab-225Ac) in combination with PNT2002 for Progressive Metastatic Castration-Resistant Prostate Cancer | Antibodies

Convergent Therapeutics and Point Biopharma Announce a Collaboration to Evaluate CONV 01-α (Rosopatamab-225Ac) in combination with PNT2002 for Progressive Metastatic Castration-Resistant Prostate Cancer | Antibodies
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United kingdomUnited statesBernard josephine chausJoe mccannScottt tagawaPhilip kantoffI convergent therapeutics incCornell universityBiopharma global incConvergent therapeutics incConvergent therapeuticsPoint biopharma announceInitiated trialWeill cornell medicinePrincipal investigatorUnited statesi september