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Taking people in Dánia1. fázis

Open-label Study of BBO-8520 in Adult Subjects With KRASG12C Non-small Cell Lung Cancer

Key facts

Where
Copenhagen, DániaSee the site
Phase
1. fázis

Where in Dánia

  • RigshospitaletCopenhagen, DániaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
TheRas, Inc., d/b/a BBOT (BridgeBio Oncology Therapeutics)
Trial code
NCT06343402
Record updated
2026. szeptember 3.
Original description
A first in human study to evaluate the safety and preliminary antitumor activity of BBO-8520, a KRAS G12C (ON and OFF) inhibitor, as a single agent and in combination with pembrolizumab and BBO-10203 in subjects with locally advanced and unresectable or metastatic non-small cell lung cancer with a KRAS (Kirsten rat sarcoma) G12C mutation.Read full original descriptionShow less

A Phase 1a/1b Open-Label Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of BBO-8520 in Subjects With Advanced KRASG12C Mutant Non-Small Cell Lung Cancer - The ONKORAS-101 Study

A first in human study to evaluate the safety and preliminary antitumor activity of BBO-8520, a KRAS G12C (ON and OFF) inhibitor, as a single agent and in combination with pembrolizumab and BBO-10203 in subjects with locally advanced and unresectable or metastatic non-small cell lung cancer with a KRAS (Kirsten rat sarcoma) G12C mutation.

Inclusion: Histologically documented locally advanced and unresectable or metastatic non-small cell lung cancer with a KRAS G12C mutation; Measurable disease by RECIST v1.1; Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-1.

Exclusion: Patients with malignancy within the last 2 years as specified in the protocol; Patients with known hypersensitivity to BBO-8520 or its excipients; Patients with a known hypersensitivity to pembrolizumab or its excipients; Patients with active autoimmune disease of history of autoimmune disease that might recur; Patients with a history of interstitial lung disease/pneumonitis that required steroids, or current interstitial lung disease/pneumonitis; Other inclusion/exclusion criteria may apply; Patients with untreated or unstable brain metastases; For Cohorts 1b and 2b:.

ClinicalTrials.gov NCT06343402