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FDA grands second approval for AbbVie’s EPKINLY in follicular lymphoma Genmab
PremiumThe FlyFDA grands second approval for AbbVie’s EPKINLY in follicular lymphoma Genmab
8d ago
EPKINLY® (epcoritamab-bysp) Approved by U.S. FDA for Patients with Relapsed or Refractory (R/R) Follicular Lymphoma (FL)
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EPKINLY® (epcoritamab-bysp) Approved by U.S. FDA for Patients with Relapsed or Refractory (R/R) Follicular Lymphoma (FL)
8d ago
Genmab’s  Epkinly gets FDA accelerated approval for lymphoma
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Genmab’s Epkinly gets FDA accelerated approval for lymphoma
8d ago
Grant of Restricted Stock Units and Warrants to Employees in Genmab
PremiumPress ReleasesGrant of Restricted Stock Units and Warrants to Employees in Genmab
22d ago
Transactions with shares and linked securities in Genmab A/S made by managerial employees and their closely associated persons
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Transactions with shares and linked securities in Genmab A/S made by managerial employees and their closely associated persons
23d ago
Transactions in Connection with Share Buy-back Program
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Transactions in Connection with Share Buy-back Program
24d ago
Investigational Tisotumab Vedotin Phase 2 Data Demonstrates Encouraging Antitumor Activity in Patients with Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma (HNSCC)
PremiumPress ReleasesInvestigational Tisotumab Vedotin Phase 2 Data Demonstrates Encouraging Antitumor Activity in Patients with Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma (HNSCC)
1M ago
Genmab announces efficacy, safety data from ongoing Phase 1/2 clinical trials
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Genmab announces efficacy, safety data from ongoing Phase 1/2 clinical trials
1M ago
Preliminary Analysis of Data Evaluating Investigational Epcoritamab (DuoBody® CD3xCD20) Combination Demonstrates 95% Overall Response Rate in Patients with Previously Untreated Follicular Lymphoma
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Preliminary Analysis of Data Evaluating Investigational Epcoritamab (DuoBody® CD3xCD20) Combination Demonstrates 95% Overall Response Rate in Patients with Previously Untreated Follicular Lymphoma
1M ago

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