Phase 1, First-in-human, Open-label Dose Escalation and Cohort Expansion Study of KB-0742 in Patients With Relapsed or Refractory Solid Tumors or Non-Hodgkin Lymphoma
Latest Information Update: 25 Jul 2024
At a glance
- Drugs KB-0742 (Primary)
- Indications Adenoid cystic carcinoma; Carcinoma; Chordoma; Diffuse large B cell lymphoma; Ewing's sarcoma; Liposarcoma; Non-Hodgkin's lymphoma; Non-small cell lung cancer; Ovarian cancer; Rhabdomyosarcoma; Sarcoma; Small cell lung cancer; Soft tissue sarcoma; Solid tumours; Triple negative breast cancer
- Focus Adverse reactions; First in man; Proof of concept
- Sponsors Kronos Bio
- 23 Jul 2024 According to a Kronos Bio media release, the first patient dosed in an expansion cohort with KB-0742 at a dose of 80mg given on a four-days-on, three-days-off schedule.
- 04 Jun 2024 Results ( As of January 4, 2024, n=112) assessing pdated KB-0742 safety, pharmacokinetics (PK), pharmacodynamic data (PD) and anti-tumor activity for patients from the ongoing dose escalation through 5 dose levels and 60 mg expansion, presented at the 60th Annual Meeting of the American Society of Clinical Oncology.
- 09 May 2024 According to a Kronos Bio media release, company presented posters of A dose escalation and cohort expansion study of the CDK9 inhibitor KB-0742 in relapsed, refractory and transcriptionally addicted solid tumors at the American Association for Cancer Research (AACR) Annual Meeting in April 2024.