-

Novellus and Tempus Announce Collaboration to Accelerate Clinical Trial Patient Enrollment

JERUSALEM--(BUSINESS WIRE)--Today Novellus, Ltd., a clinical-stage biotechnology company focused on precision oncology, and Tempus, a leader in artificial intelligence and precision medicine, announced their collaboration to accelerate patient enrollment for Novellus’ next generation BRAF inhibitor program.

Novellus’ BRAF program focuses on patient populations for which there are currently no FDA-approved BRAF inhibitors, including BRAF fusions and BRAF-mutated gliomas. Novellus will participate in Tempus’s TIME Trial® Network, and the companies will work together to identify relevant patients to accelerate patient enrollment.

“The collaboration with Tempus will enable us to accelerate the enrollment of patients in our BRAF trial, by precisely identifying potential candidates and opening sites wherever the patients are found” said Michael Vidne, Chief Executive Officer of Novellus.

“The TIME Trial Program has achieved an unparalleled scale thus far, with over 50 provider networks and 2,500 oncologists included in its network,” said Kim Blackwell, Chief Medical Officer of Tempus. “We’re excited to collaborate with Novellus, to further our mission to increase trial participation, and to ultimately bring the right treatment to the right patients at the right time.”

About Novellus, Ltd.
Novellus is a clinical-stage drug development company. Novellus focuses on the development of compounds for established oncogene drivers with a high incidence of uncharacterized mutations. Novellus’ BRAF program is in clinical trial (NCT02428712).

Contacts

Novellus, Ltd.
Yaron Shimon
Yaron@Novellus.Bio

Novellus


Release Versions

Contacts

Novellus, Ltd.
Yaron Shimon
Yaron@Novellus.Bio

More News From Novellus

FORE Biotherapeutics Announces Two Abstracts Accepted for Presentation at the 2023 American Society of Clinical Oncology (ASCO) Annual Meeting

PHILADELPHIA--(BUSINESS WIRE)--FORE Biotherapeutics today announced the acceptance of two abstracts on new clinical data related to FORE8394, the company's novel, investigational, small-molecule, next-generation, orally available selective inhibitor of BRAF alterations at the American Society of Clinical Oncology (ASCO) Annual Meeting, taking place June 3-7, 2023, in Chicago and virtually. The datasets from the phase 1/2a clinical trial, evaluating the safety, tolerability, and efficacy of FORE...

FORE Biotherapeutics Receives FDA Orphan Drug Designation for FORE8394 for the Treatment of Primary Brain and CNS Malignancies

PHILADEPHIA--(BUSINESS WIRE)--FORE Biotherapeutics (FORE Bio) a precision stage oncology company dedicated to developing innovative treatments that provide a better outcome for cancer patients announced today that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Designation (ODD) to its lead program, FORE8394, for the treatment of primary brain and central nervous system (CNS) malignancies. This is the first orphan drug designation received by FORE Bio and the FORE8394 progra...

Fore Biotherapeutics Announces First Patient Dosed in Global Phase 2 Trial Evaluating FORE8394 in BRAF-Mutated Solid and Brain Tumors

PHILADELPHIA--(BUSINESS WIRE)--FORE BIOTHERAPEUTICS ANNOUNCES FIRST PATIENT DOSED IN GLOBAL PHASE 2 TRIAL EVALUATING FORE8394 IN BRAF-MUTATED SOLID AND BRAIN TUMORS...
Back to Newsroom