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Phase classification, Trial completion date, Trial termination, Combination therapy, Metastases: A Study to Find the Best Dose of BI 905711 in Combination With Chemotherapy and to Test Whether This Dose Helps People With Advanced Gastrointestinal Cancers (clinicaltrials.gov) - Dec 13, 2023 P1, N=13, Terminated, Active, not recruiting --> Completed Phase classification: P1a/1b --> P1 | Trial completion date: Mar 2024 --> Oct 2023 | Active, not recruiting --> Terminated
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Enrollment closed, Enrollment change, Trial completion date, Trial primary completion date, Combination therapy, Metastases: A Study to Find the Best Dose of BI 905711 in Combination With Chemotherapy and to Test Whether This Dose Helps People With Advanced Gastrointestinal Cancers (clinicaltrials.gov) - Apr 18, 2023 P1a/1b, N=10, Active, not recruiting, N=10 --> 13 Recruiting --> Active, not recruiting | N=100 --> 10 | Trial completion date: Nov 2024 --> Sep 2023 | Trial primary completion date: Jun 2024 --> Sep 2023
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[VIRTUAL] BI 905711 selectively induces apoptosis and anti-tumor response in TRAILR2/CDH17- expressing pancreatic cancer models () - Mar 13, 2021 - Abstract #AACR2021AACR_4355; P1 Responders to BI 905711 were identified primarily within the classical and quasi-basal/hybrid subtypes when TRAILR2 was adequately co-expressed. This correlates with an enrichment pattern of CDH17 gene expression that is mostly within the classical gene cluster and strongly anti-correlated with basal-like cluster enrichment.Robust preclinical anti-tumor activity of BI 905711 in TRAILR2 and CDH17-expressing PDAC PDX models, along with this antibody’s potential for a favorable safety profile, has justified the enrollment of pancreatic cancer patients in the ongoing BI 905711 FIH Phase I clinical trial (NCT04137289).
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Trial completion date, Metastases: A Study to Find a Safe and Effective Dose of BI 905711 in Patients With Advanced Gastrointestinal Cancer (clinicaltrials.gov) - Jul 7, 2020 P1, N=140, Recruiting, This correlates with an enrichment pattern of CDH17 gene expression that is mostly within the classical gene cluster and strongly anti-correlated with basal-like cluster enrichment.Robust preclinical anti-tumor activity of BI 905711 in TRAILR2 and CDH17-expressing PDAC PDX models, along with this antibody’s potential for a favorable safety profile, has justified the enrollment of pancreatic cancer patients in the ongoing BI 905711 FIH Phase I clinical trial (NCT04137289). Trial completion date: Apr 2024 --> May 2023
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[VIRTUAL] Expanding the Druggable Cancer Target Space (Room 16 A-B - Mezz Lvl - SDCC) - Mar 6, 2020 - Abstract #AACR2020AACR_775; BI 1701963 is the first SOS1::KRAS inhibitor to advance to clinical trials and, in combination with RAS/MAPK pathway-targeted drugs, represents an approach to target a broad spectrum of mutant KRAS-driven cancers, including major non-G12C-mutated cancers...BI 905677 is a first-in-class LRP5/6 antagonist in phase 1 studies that effectively targets WNT-driven proliferation and immune escape...BI 905711 is scheduled to enter phase 1 clinical trials in early 2020. Collectively, these three areas of precision medicines promise to significantly expand the druggable target space and offer much-needed therapeutic options to cancer patients.
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Trial completion date, Trial primary completion date, Metastases: A Study to Find a Safe and Effective Dose of BI 905711 in Patients With Advanced Gastrointestinal Cancer (clinicaltrials.gov) - Jan 7, 2020 P1, N=140, Not yet recruiting, Collectively, these three areas of precision medicines promise to significantly expand the druggable target space and offer much-needed therapeutic options to cancer patients. Trial completion date: Jan 2023 --> Apr 2024 | Trial primary completion date: Nov 2022 --> Apr 2023
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