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MorphoSys AG: Invitation to MorphoSys' First Quarter Results Conference Call on May 6, 2021

MorphoSys AG: Invitation to MorphoSys First Quarter Results Conference Call on May 6, 2021 Invitation to MorphoSys First Quarter Results Conference Call on May 6, 2021 MUNICH, GERMANY / ACCESSWIRE / April 28, 2021 / MorphoSys AG (FSE:MOR)(NASDAQ: MOR), a commercial-stage biopharmaceutical company and a leader in antibody, protein and peptide technologies, will publish its results for the first quarter of 2021 on May 5, 2021 at 10:00pm CEST (4:00pm EDT). MorphoSys Management Board will host a co...
United Kingdom Thomas Biegi Julia Neugebauer Jean Paul Kress Myles Clouston Jeanette Bressi

Incyte and MorphoSys AG: Incyte and MorphoSys Announce First Patient Dosed in Phase 3 inMIND Study Evaluating the Addition of Tafasitamab to Lenalidomide and Rituximab in Relapsed or Refractory Follicular or Marginal Zone Lymphoma

Incyte and MorphoSys AG: Incyte and MorphoSys Announce First Patient Dosed in Phase 3 inMIND Study Evaluating the Addition of Tafasitamab to Lenalidomide and Rituximab in Relapsed or Refractory Follicular or Marginal Zone Lymphoma Respiratory tract infection These are not all the possible side effects of MONJUVI. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. Before you receive MONJUVI, tell your healthcare provider about all your m...
United States Julia Neugebauer Peter Langmuir Mike Akimov Myles Clouston Jeanette Bressi

MorphoSys AG: MorphoSys and Incyte Announce First Patient Dosed in Phase 3 inMIND Study Evaluating the Addition of Tafasitamab to Lenalidomide and Rituximab in Relapsed or Refractory Follicular or Marginal Zone Lymphoma

MorphoSys AG: MorphoSys and Incyte Announce First Patient Dosed in Phase 3 inMIND Study Evaluating the Addition of Tafasitamab to Lenalidomide and Rituximab in Relapsed or Refractory Follicular or Marginal Zone Lymphoma Respiratory tract infection These are not all the possible side effects of MONJUVI. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. Before you receive MONJUVI, tell your healthcare provider about all your medical cond...
United States Julia Neugebauer Peter Langmuir Mike Akimov Myles Clouston Jeanette Bressi

MorphoSys AG: Invitation to MorphoSys' Full Year Results 2020 Conference Call on March 16, 2021

MorphoSys AG: Invitation to MorphoSys Full Year Results 2020 Conference Call on March 16, 2021 Conference Call Alert PLANEGG & MUNICH, GERMANY / ACCESSWIRE / March 9, 2021 / MorphoSys AG (FSE:MOR; Prime Standard Segment; MDAX & TecDAX; NASDAQ:MOR), a commercial-stage biopharmaceutical company and a leader in antibody, protein, and peptide technologies, will publish its results for the financial year 2020 on March 15, 2021 at 10:00 pm CET (5:00 pm EDT). MorphoSys Management team will host a conf...
United Kingdom Thomas Biegi Julia Neugebauer Jean Paul Kress Myles Clouston Jeanette Bressi

I-Mab and MorphoSys Announce First Patient Dosed in U.S. Phase 1 Study of TJ210/MOR210 in Patients with Advanced Cancer

Share this article Share this article SHANGHAI, China and PLANEGG/MUNICH, Germany, Jan. 25, 2021 /PRNewswire/ -- I-Mab (Nasdaq: IMAB), and MorphoSys (FSE: MOR; Prime Standard Segment, MDAX & TecDAX;NASDAQ: MOR) today announced that the first patient has been dosed in a phase 1 dose escalation study to evaluate the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of TJ210/MOR210 monotherapy in patients with relapsed or refractory advanced solid tumors in the United States. ...
United States Hong Kong San Diego South Korea Thomas Biegi Julia Neugebauer

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MorphoSys AG: MorphoSys and I-Mab Announce First Patient Dosed in U.S. Phase 1 Study of MOR210/TJ210 in Patients with Advanced Cancer

(3) PLANEGG/MUNICH, GERMANY and SHANGHAI, CHINA / ACCESSWIRE / January 25, 2021 / MorphoSys (FSE:MOR)(Prime Standard Segment, MDAX & TecDAX)(NASDAQ:MOR) and I-Mab (IMAB) today announced that the first patient has been dosed in a phase 1 dose escalation study to evaluate the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of MOR210/ TJ210 monotherapy in patients with relapsed or refractory advanced solid tumors in the United States. MOR210/TJ210 is a monoclonal antibody dev...
United States Hong Kong San Diego South Korea Thomas Biegi Julia Neugebauer

MorphoSys and Incyte Announce Acceptance by Health Canada of the New Drug Submission for Tafasitamab

Press release content from Accesswire. The AP news staff was not involved in its creation. MorphoSys and Incyte Announce Acceptance by Health Canada of the New Drug Submission for Tafasitamab January 12, 2021 GMT PLANEGG/MUNICH, GERMANY and MONTREAL, QC / ACCESSWIRE / January 12, 2021 / MorphoSys AG (FSE:MOR; Prime Standard Segment; MDAX & TecDAX; NASDAQ:MOR) and Incyte (NASDAQ:INCY) today announced that Health Canada has accepted the New Drug Submission (NDS) for tafasitamab, an anti-CD19 anti...
United States Nuwan Kurukulasuriya Jeanette Bressi Global Medical Affairs Practice Research Clinical Haematology Janssen Biotech Inc
Source: apnews.com

MorphoSys AG: MorphoSys and Incyte Announce Acceptance by Health Canada of the New Drug Submission for Tafasitamab

(2) PLANEGG/MUNICH, GERMANY and MONTREAL, QC / ACCESSWIRE / January 12, 2021 / MorphoSys AG (FSE:MOR; Prime Standard Segment; MDAX & TecDAX; NASDAQ:MOR) and Incyte (NASDAQ:INCY) today announced that Health Canada has accepted the New Drug Submission (NDS) for tafasitamab, an anti-CD19 antibody. The application seeks approval of tafasitamab in combination with lenalidomide, followed by tafasitamab monotherapy, for the treatment of adult patients with relapsed or refractory diffuse large B-cell l...
United States Julia Neugebauer Myles Clouston Jeanette Bressi Thomas Biegi Catalina Loveman

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