Deleted in Colorectal Cancer

Merck KGaA, Darmstadt, Germany Aims to Double R&D Productivity in Oncology, Neurology and Immunology to Deliver More Medicines to Patients Faster

Retrieved on: 
Monday, November 21, 2022

Xevinapant, which was in-licensed from Debiopharm in March 2021, builds on the companys long heritage and extensive expertise in SCCHN.

Key Points: 
  • Xevinapant, which was in-licensed from Debiopharm in March 2021, builds on the companys long heritage and extensive expertise in SCCHN.
  • M1774 has broad potential in combination with other DDR inhibitors and other medicines, and as monotherapy in the right genomic context.
  • Merck KGaA, Darmstadt, Germany, a leading science and technology company, operates across life science, healthcare and electronics.
  • Since its founding in 1668, scientific exploration and responsible entrepreneurship have been key to the companys technological and scientific advances.

Merck Aims to Double R&D Productivity in Oncology, Neurology and Immunology to Deliver More Medicines to Patients Faster

Retrieved on: 
Monday, November 21, 2022

Merck, a leading science and technology company, today shared updates on the companys healthcare research and development strategy, aimed at doubling R&D productivity.

Key Points: 
  • Merck, a leading science and technology company, today shared updates on the companys healthcare research and development strategy, aimed at doubling R&D productivity.
  • Xevinapant, which was in-licensed from Debiopharm in March 2021, builds on the companys long heritage and extensive expertise in SCCHN.
  • M1774 has broad potential in combination with other DDR inhibitors and other medicines, and as monotherapy in the right genomic context.
  • Building on expertise in neurology, the company is initiating a proof-of-concept study in neuromuscular conditions dermatomyositis and polymyositis with enpatoran in 2023.

Pushing past pancreatic tumors' defenses

Retrieved on: 
Wednesday, February 16, 2022

Cancer cells weave a deactivating signal into a protective coat of armor that excludes T cells that would otherwise kill them.

Key Points: 
  • Cancer cells weave a deactivating signal into a protective coat of armor that excludes T cells that would otherwise kill them.
  • This immune deactivation pathway offers a promising new therapeutic approach for pancreatic, breast, and colorectal cancers.
  • The scientists used genetic editing to turn off the production of KRT19 or TGM2 in mouse pancreatic tumors.
  • In a previous small clinical study of pancreatic cancer patients, Fearon and collaborators showed that the drug plerixafor (a CXCL12 receptor blocker) increased the infiltration of T cells into patients' pancreatic tumor tissues.

Qurient Announces U.S. FDA Clearance of IND Application for Q901, a Novel Cancer Therapy

Retrieved on: 
Tuesday, February 8, 2022

IND clearance for Q901 is an important step forward in developing this novel drug candidate that may provide a new alternative treatment to patients with relapsed or refractory malignancies, says Kiyean Nam, Ph.D., CEO of Qurient.

Key Points: 
  • IND clearance for Q901 is an important step forward in developing this novel drug candidate that may provide a new alternative treatment to patients with relapsed or refractory malignancies, says Kiyean Nam, Ph.D., CEO of Qurient.
  • Additional data from preclinical studies has demonstrated that selective inhibition of CDK7 specifically kills cancer cells with aberrant cell division cycle or transcriptional regulation.
  • Qurient licensed the CDK7 inhibitor program at lead stage from Lead Discovery Center (LDC) and the Max-Planck Society and further optimized the program, completed the IND-enabling studies, and submitted the IND application.
  • Qurient mainly focuses on development of novel therapeutics from discovery to human proof of concept stages through virtual R&D project management platform.

Privo Technologies, Inc. Announces Positive Results From Phase 1/2 Clinical Trial for PRV111 in Head and Neck Squamous Cell Carcinoma

Retrieved on: 
Friday, October 22, 2021

PRV111 showed a favorable safety profile with no severe adverse events (SAEs).

Key Points: 
  • PRV111 showed a favorable safety profile with no severe adverse events (SAEs).
  • Reported treatment emergent adverse events (TEAEs) were mild or moderate in severity, and no dose-limiting toxicities (DLTs) were observed.
  • The clinical trial design was Open-Label, Single-Arm Safety, Tolerability, Anti-Tumor Effects, Systemic Exposure, and Device Technical Effects of PRV111 in subjects with Head and Neck Squamous Cell Carcinoma.
  • Squamous cell carcinoma (SCC) is cancer of the squamous cells - thin and flat cells that line the epithelia.