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BIOMARKER:

EGFR wild-type + ALK wild-type

i
Other names: EGFR, ERBB, ERBB1, Epidermal growth factor receptor, NBLST3, CD246, Anaplastic Lymphoma Kinase, Anaplastic Lymphoma Kinase (Ki-1), CD246 Antigen, Mutant Anaplastic Lymphoma Kinase, ALK, ALK Receptor Tyrosine Kinase, Anaplastic Lymphoma Receptor Tyrosine Kinase, ALK Tyrosine Kinase Receptor
Entrez ID:
2ms
SI-B001 Combined With Chemotherapy in the Treatment of EGFR/ALK WT Recurrent or Metastatic NSCLC. (clinicaltrials.gov)
P2, N=60, Recruiting, Sichuan Baili Pharmaceutical Co., Ltd. | Trial completion date: Aug 2024 --> Jun 2025 | Trial primary completion date: Aug 2024 --> Jun 2025
Trial completion date • Trial primary completion date • Combination therapy • Metastases
|
EGFR (Epidermal growth factor receptor) • ALK (Anaplastic lymphoma kinase)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
cisplatin • paclitaxel • docetaxel • pemetrexed • izalontamab (SI-B001)
3ms
Proteogenomic characterization identifies clinical subgroups in EGFR and ALK wild-type never-smoker lung adenocarcinoma. (PubMed, Exp Mol Med)
Upregulated cytokines, such as CCL5 and CXCL13, in the immune subgroup may serve as potential targets for combination immunotherapy. Our comprehensive proteogenomic analysis revealed the molecular subtypes of EGFR- and ALK-wild-type NSLA with significant unmet clinical needs.
Journal • IO biomarker
|
EGFR (Epidermal growth factor receptor) • ALK (Anaplastic lymphoma kinase) • CXCL13 (Chemokine (C-X-C motif) ligand 13)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
3ms
SILK BM: A Trial Evaluating Stereotactic Radiotherapy Plus Durvalumab Continuation for Patients With NSCLC Metachronous Oligometastatic Disease Under Durvalumab Consolidation Following Chemoradiation (clinicaltrials.gov)
P2, N=4, Completed, Institut Claudius Regaud | Active, not recruiting --> Completed | Trial completion date: Dec 2025 --> Aug 2024 | Trial primary completion date: Dec 2025 --> Aug 2024
Trial completion • Trial completion date • Trial primary completion date
|
EGFR (Epidermal growth factor receptor) • ALK (Anaplastic lymphoma kinase) • CTLA4 (Cytotoxic T-Lymphocyte Associated Protein 4)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
Imfinzi (durvalumab)
9ms
AK105-301: A Study of Anti-PD-1 AK105 in Patients With Metastatic Nonsquamous Non-small Cell Lung Cancer (clinicaltrials.gov)
P3, N=164, Terminated, Akeso | Trial completion date: Jun 2024 --> Dec 2023 | Active, not recruiting --> Terminated; corporate strategy adjustment
Trial completion date • Trial termination • Metastases
|
EGFR (Epidermal growth factor receptor)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
carboplatin • Focus V (anlotinib) • pemetrexed • Anniko (penpulimab)
10ms
Enrollment open • Trial primary completion date • Surgery
|
EGFR (Epidermal growth factor receptor)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
Imfinzi (durvalumab)
10ms
Enrollment open • Combination therapy • Metastases
|
EGFR wild-type • EGFR wild-type + ALK wild-type
|
izalontamab brengitecan (BL-B01D1) • danvilostomig (SI-B003)
10ms
PACIFIC-8: A Global Study to Assess the Effects of Durvalumab + Domvanalimab Following Concurrent Chemoradiation in Participants With Stage III Unresectable NSCLC (clinicaltrials.gov)
P3, N=860, Recruiting, AstraZeneca | Trial completion date: Sep 2029 --> Aug 2030 | Trial primary completion date: Jun 2027 --> Jun 2028
Trial completion date • Trial primary completion date • Metastases
|
EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
Imfinzi (durvalumab) • domvanalimab (AB154)
10ms
SI-B001 Combined With Chemotherapy in the Treatment of EGFR/ALK WT Recurrent or Metastatic NSCLC. (clinicaltrials.gov)
P2, N=60, Recruiting, Sichuan Baili Pharmaceutical Co., Ltd. | Trial completion date: Dec 2023 --> Apr 2024 | Trial primary completion date: Dec 2023 --> Apr 2024
Trial completion date • Trial primary completion date • Combination therapy • Metastases
|
EGFR (Epidermal growth factor receptor) • ALK (Anaplastic lymphoma kinase)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
cisplatin • paclitaxel • docetaxel • pemetrexed • izalontamab (SI-B001)
11ms
Phase Ib Study of TNO155 in Combination With Spartalizumab or Ribociclib in Selected Malignancies (clinicaltrials.gov)
P1, N=122, Terminated, Novartis Pharmaceuticals | Active, not recruiting --> Terminated; Business reasons
Trial termination • Combination therapy
|
EGFR (Epidermal growth factor receptor) • KRAS (KRAS proto-oncogene GTPase)
|
KRAS G12C • EGFR wild-type • KRAS wild-type • RAS wild-type • KRAS G12 • EGFR wild-type + ALK wild-type
|
Kisqali (ribociclib) • spartalizumab (PDR001) • batoprotafib (TNO155)
12ms
Enrollment change • Combination therapy • Metastases
|
EGFR wild-type • EGFR wild-type + ALK wild-type
|
izalontamab brengitecan (BL-B01D1) • danvilostomig (SI-B003)
1year
Trial completion date • Trial initiation date • Trial primary completion date • Metastases
|
EGFR wild-type • EGFR wild-type + ALK wild-type
|
izalontamab brengitecan (BL-B01D1) • danvilostomig (SI-B003)
1year
Trial completion date • Trial primary completion date • Surgery
|
EGFR (Epidermal growth factor receptor)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
Imfinzi (durvalumab)
over1year
Enrollment open
|
EGFR (Epidermal growth factor receptor) • HER-2 (Human epidermal growth factor receptor 2) • KRAS (KRAS proto-oncogene GTPase) • BRAF (B-raf proto-oncogene) • ALK (Anaplastic lymphoma kinase) • ROS1 (Proto-Oncogene Tyrosine-Protein Kinase ROS) • NTRK (Neurotrophic receptor tyrosine kinase)
|
KRAS mutation • KRAS G12C • BRAF mutation • HER-2 amplification • BRAF V600 • KRAS G12D • EGFR wild-type • KRAS G12V • RET mutation • ALK wild-type • ROS1 fusion • ROS1 rearrangement • MET mutation • RET rearrangement • KRAS G12 • EGFR wild-type + ALK wild-type • KRAS amplification • NTRK fusion
|
docetaxel • izalontamab (SI-B001)
over1year
ZWI-ZW25-101: Trial of ZW25 (Zanidatamab) in Patients With Advanced HER2-expressing Cancers (clinicaltrials.gov)
P1, N=279, Active, not recruiting, Jazz Pharmaceuticals | Trial completion date: Aug 2023 --> Jul 2024 | Trial primary completion date: Jun 2023 --> Jun 2024
Trial completion date • Trial primary completion date • Metastases
|
EGFR (Epidermal growth factor receptor) • HER-2 (Human epidermal growth factor receptor 2) • KRAS (KRAS proto-oncogene GTPase) • ALK (Anaplastic lymphoma kinase) • ROS1 (Proto-Oncogene Tyrosine-Protein Kinase ROS)
|
HER-2 positive • HER-2 overexpression • EGFR wild-type • KRAS wild-type • ALK wild-type • RAS wild-type • EGFR wild-type + ALK wild-type • ALK-ROS1 fusion
|
paclitaxel • capecitabine • Tukysa (tucatinib) • vinorelbine tartrate • Ziihera (zanidatamab-hrii)
over1year
New P2 trial • Metastases
|
EGFR wild-type • EGFR wild-type + ALK wild-type
|
izalontamab brengitecan (BL-B01D1) • danvilostomig (SI-B003)
over1year
New P3 trial
|
EGFR (Epidermal growth factor receptor) • HER-2 (Human epidermal growth factor receptor 2) • KRAS (KRAS proto-oncogene GTPase) • BRAF (B-raf proto-oncogene) • ALK (Anaplastic lymphoma kinase) • ROS1 (Proto-Oncogene Tyrosine-Protein Kinase ROS) • NTRK (Neurotrophic receptor tyrosine kinase)
|
KRAS mutation • KRAS G12C • BRAF mutation • HER-2 amplification • BRAF V600 • KRAS G12D • EGFR wild-type • KRAS G12V • RET mutation • ALK wild-type • ROS1 fusion • ROS1 rearrangement • MET mutation • RET rearrangement • KRAS G12 • EGFR wild-type + ALK wild-type • KRAS amplification • NTRK fusion
|
docetaxel • izalontamab (SI-B001)
over1year
Treatment patterns and outcomes of patients with metastatic non-small cell lung cancer in five European countries: a real-world evidence survey. (PubMed, BMC Cancer)
Real-world treatment patterns suggest that chemotherapy use remains high despite guidelines recommending immunotherapy-based 1L treatment for mNSCLC. QoL reported by patients was generally lower than population reference values. Not implying causality, 1L immunotherapy use was higher during COVID-19 than pre-COVID-19, and the UK saw the biggest impact to patient management due to COVID-19.
Journal • HEOR • Real-world evidence • PD(L)-1 Biomarker • IO biomarker • Real-world • Metastases
|
EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1) • ALK (Anaplastic lymphoma kinase)
|
PD-L1 expression • EGFR wild-type • ALK mutation • ALK wild-type • EGFR wild-type + ALK wild-type • EGFR mutation + ALK mutation
over1year
New P2 trial • Surgery
|
EGFR (Epidermal growth factor receptor)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
Imfinzi (durvalumab)
over1year
PEOPLE (NTC03447678), a phase II trial to test pembrolizumab as first-line treatment in patients with advanced NSCLC with PD-L1 <50%: a multiomics analysis. (PubMed, J Immunother Cancer)
P=N/A; This multiomics approach was able to identify immune cell subsets and expression levels of genes associated to PFS in patients with PD-L1 <50% NSCLC treated with first-line pembrolizumab. These preliminary data will be confirmed in the larger multicentric international I3LUNG trial (NCT05537922).
Journal • P2 data • PD(L)-1 Biomarker • IO biomarker • Metastases
|
EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1) • ALK (Anaplastic lymphoma kinase) • PTPRC (Protein Tyrosine Phosphatase Receptor Type C) • KLRB1 (Killer Cell Lectin Like Receptor B1)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
nCounter® PanCancer IO 360™ Panel
|
Keytruda (pembrolizumab)
over1year
Cost-effectiveness evaluation based on two models of first-line atezolizumab monotherapy and chemotherapy for advanced non-small cell lung cancer with high-PDL1 expression. (PubMed, Front Oncol)
In some areas of China with higher levels of economic development, atezolizumab was likely to be cost-effective. To improve the cost-effectiveness of atezolizumab, drug prices would need to be reduced.
Journal • HEOR • PD(L)-1 Biomarker • IO biomarker • Cost-effectiveness • Cost effectiveness • Metastases
|
EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1)
|
PD-L1 expression • PD-L1 overexpression • EGFR expression • EGFR wild-type • EGFR overexpression • ALK wild-type • EGFR wild-type + ALK wild-type
|
Tecentriq (atezolizumab)
over1year
Phase Ib Study of TNO155 in Combination With Spartalizumab or Ribociclib in Selected Malignancies (clinicaltrials.gov)
P1, N=122, Active, not recruiting, Novartis Pharmaceuticals | Recruiting --> Active, not recruiting | N=185 --> 122 | Trial completion date: Apr 2025 --> Oct 2023 | Trial primary completion date: Apr 2025 --> Oct 2023
Enrollment closed • Enrollment change • Trial completion date • Trial primary completion date • Combination therapy
|
EGFR (Epidermal growth factor receptor) • KRAS (KRAS proto-oncogene GTPase)
|
KRAS G12C • EGFR wild-type • KRAS wild-type • RAS wild-type • KRAS G12 • EGFR wild-type + ALK wild-type
|
Kisqali (ribociclib) • spartalizumab (PDR001) • batoprotafib (TNO155)
almost2years
Enrollment closed • Enrollment change • Metastases
|
EGFR (Epidermal growth factor receptor) • ALK (Anaplastic lymphoma kinase) • CTLA4 (Cytotoxic T-Lymphocyte Associated Protein 4)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
Imfinzi (durvalumab)
2years
Phase Ib Study of TNO155 in Combination With Spartalizumab or Ribociclib in Selected Malignancies (clinicaltrials.gov)
P1, N=185, Recruiting, Novartis Pharmaceuticals | Trial completion date: Sep 2024 --> Apr 2025 | Trial primary completion date: Sep 2024 --> Apr 2025
Trial completion date • Trial primary completion date • Combination therapy
|
EGFR (Epidermal growth factor receptor) • KRAS (KRAS proto-oncogene GTPase)
|
KRAS G12C • EGFR wild-type • KRAS wild-type • RAS wild-type • KRAS G12 • EGFR wild-type + ALK wild-type
|
Kisqali (ribociclib) • spartalizumab (PDR001) • batoprotafib (TNO155)
2years
ZWI-ZW25-101: Trial of ZW25 (Zanidatamab) in Patients With Advanced HER2-expressing Cancers (clinicaltrials.gov)
P1, N=279, Active, not recruiting, Zymeworks Inc. | Trial completion date: Oct 2022 --> Aug 2023 | Trial primary completion date: Sep 2022 --> Jun 2023
Trial completion date • Trial primary completion date • Metastases
|
EGFR (Epidermal growth factor receptor) • HER-2 (Human epidermal growth factor receptor 2) • KRAS (KRAS proto-oncogene GTPase) • ALK (Anaplastic lymphoma kinase) • ROS1 (Proto-Oncogene Tyrosine-Protein Kinase ROS)
|
HER-2 positive • HER-2 overexpression • EGFR wild-type • KRAS wild-type • ALK wild-type • RAS wild-type • EGFR wild-type + ALK wild-type • ALK-ROS1 fusion
|
paclitaxel • capecitabine • Tukysa (tucatinib) • vinorelbine tartrate • Ziihera (zanidatamab-hrii)
2years
AK105-301: A Study of Anti-PD-1 AK105 in Patients With Metastatic Nonsquamous Non-small Cell Lung Cancer (clinicaltrials.gov)
P3, N=164, Active, not recruiting, Akeso | Unknown status --> Active, not recruiting | N=360 --> 164 | Trial completion date: Nov 2021 --> Jun 2024 | Trial primary completion date: Nov 2020 --> Jun 2023
Enrollment closed • Enrollment change • Trial completion date • Trial primary completion date • Metastases
|
EGFR (Epidermal growth factor receptor)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
carboplatin • Focus V (anlotinib) • pemetrexed • Anniko (penpulimab)
over2years
New P3 trial
|
EGFR (Epidermal growth factor receptor)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
Imfinzi (durvalumab) • docetaxel • ceralasertib (AZD6738)
over2years
Association Between EGFR and ALK Mutation Status on Patient-Reported Symptoms After Palliative Radiation for Bone Pain in NSCLC. (PubMed, JTO Clin Res Rep)
ALK+ mutation status was associated with a higher rate of complete response compared with WT (OR = 5.2, p = 0.031). There was an association between EGFR+ and ALK+ tumors and increased rates of partial pain response to palliative radiotherapy.
Journal
|
EGFR (Epidermal growth factor receptor) • ALK (Anaplastic lymphoma kinase)
|
EGFR mutation • ALK rearrangement • EGFR wild-type • ALK mutation • ALK wild-type • EGFR wild-type + ALK wild-type • EGFR mutation + ALK mutation
over2years
New P3 trial • IO biomarker
|
EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1)
|
PD-L1 expression • EGFR mutation • EGFR wild-type • ALK mutation • ALK wild-type • EGFR wild-type + ALK wild-type • PD-L1 deletion
|
Imfinzi (durvalumab) • oleclumab (MEDI9447) • monalizumab (IPH2201)
over2years
PEOPLE (NTC03447678), a phase II trial of first-line, single-agent pembrolizumab in advanced NSCLC with low PD-L1: Clinical outcomes and association with circulating immune biomarkers. (ASCO 2022)
This trial confirmed that pembrolizumab as first-line single agent is safe and active also in a subgroup of aNSCLC patients with PD-L1 < 50%. CIP biomarkers can be useful to identify patients with a favourable outcome, thus avoiding the adding toxicity of chemotherapy.
Clinical • Clinical data • P2 data • PD(L)-1 Biomarker • IO biomarker
|
EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1) • ALK (Anaplastic lymphoma kinase) • CD19 (CD19 Molecule) • NCAM1 (Neural cell adhesion molecule 1)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type • CD19 expression
|
Keytruda (pembrolizumab)
over2years
PEOPLE (NTC03447678), a phase II trial to test pembrolizumab as first-line treatment in patients with advanced NSCLC with PD-L1 < 50%: A multiomics approach. (ASCO 2022)
To the best of our knowledge, this is the first prospective trial in NSCLC with PD-L1 < 50% performed with a multi-omic approach able to identify immune cell subsets and expression levels of genes associated to PFS under first line treatment with pembrolizumab.
P2 data • Clinical • PD(L)-1 Biomarker • IO biomarker
|
EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1) • ALK (Anaplastic lymphoma kinase) • PTPRC (Protein Tyrosine Phosphatase Receptor Type C) • KLRB1 (Killer Cell Lectin Like Receptor B1)
|
PD-L1 expression • EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
nCounter® PanCancer IO 360™ Panel
|
Keytruda (pembrolizumab)
over2years
New P3 trial
|
EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
PD-L1 IHC 22C3 pharmDx
|
Imfinzi (durvalumab) • domvanalimab (AB154)
over2years
SI-B001 Combined With Chemotherapy in the Treatment of EGFR/ALK WT Recurrent or Metastatic NSCLC. (clinicaltrials.gov)
P2, N=60, Recruiting, Sichuan Baili Pharmaceutical Co., Ltd. | Phase classification: P2/3 --> P2
Phase classification • Combination therapy
|
EGFR (Epidermal growth factor receptor) • ALK (Anaplastic lymphoma kinase)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
cisplatin • paclitaxel • docetaxel • pemetrexed • izalontamab (SI-B001)
over2years
PACIFIC-8: A Global Study to Assess the Effects of Durvalumab + Domvanalimab Following Concurrent Chemoradiation in Participants With Stage III Unresectable NSCLC (clinicaltrials.gov)
P3, N=860, Recruiting, AstraZeneca | Not yet recruiting --> Recruiting | Trial primary completion date: Mar 2026 --> Jun 2027
Enrollment open • Trial primary completion date
|
EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
Imfinzi (durvalumab) • domvanalimab (AB154)
over2years
Trial completion date • IO biomarker
|
EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1)
|
PD-L1 expression • EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
Imfinzi (durvalumab) • oleclumab (MEDI9447) • monalizumab (IPH2201)
over2years
Enrollment change • Combination therapy
|
EGFR (Epidermal growth factor receptor) • KRAS (KRAS proto-oncogene GTPase) • ALK (Anaplastic lymphoma kinase)
|
KRAS G12C • EGFR wild-type • KRAS wild-type • RAS wild-type • KRAS G12 • EGFR wild-type + ALK wild-type
|
Kisqali (ribociclib) • spartalizumab (PDR001) • batoprotafib (TNO155)
almost3years
ZWI-ZW25-101: Trial of ZW25 (Zanidatamab) in Patients With Advanced HER2-expressing Cancers (clinicaltrials.gov)
P1, N=279, Active, not recruiting, Zymeworks Inc. | Recruiting --> Active, not recruiting | N=418 --> 279 | Trial completion date: Mar 2022 --> Oct 2022 | Trial primary completion date: Jan 2022 --> Sep 2022
Enrollment closed • Enrollment change • Trial completion date • Trial primary completion date
|
EGFR (Epidermal growth factor receptor) • HER-2 (Human epidermal growth factor receptor 2) • KRAS (KRAS proto-oncogene GTPase) • ALK (Anaplastic lymphoma kinase) • ROS1 (Proto-Oncogene Tyrosine-Protein Kinase ROS)
|
HER-2 positive • HER-2 overexpression • EGFR wild-type • KRAS wild-type • ALK wild-type • RAS wild-type • EGFR wild-type + ALK wild-type • ALK-ROS1 fusion
|
paclitaxel • capecitabine • Tukysa (tucatinib) • vinorelbine tartrate • Ziihera (zanidatamab-hrii)
almost3years
Enrollment open • IO biomarker
|
EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1)
|
PD-L1 expression • EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
Imfinzi (durvalumab) • oleclumab (MEDI9447) • monalizumab (IPH2201)
almost3years
Phase Ib Study of TNO155 in Combination With Spartalizumab or Ribociclib in Selected Malignancies (clinicaltrials.gov)
P1, N=126, Recruiting, Novartis Pharmaceuticals | Trial completion date: Oct 2023 --> Sep 2024 | Trial primary completion date: Oct 2023 --> Sep 2024
Trial completion date • Trial primary completion date • Combination therapy
|
EGFR (Epidermal growth factor receptor) • KRAS (KRAS proto-oncogene GTPase) • ALK (Anaplastic lymphoma kinase)
|
KRAS G12C • EGFR wild-type • KRAS wild-type • RAS wild-type • KRAS G12 • EGFR wild-type + ALK wild-type
|
Kisqali (ribociclib) • spartalizumab (PDR001) • batoprotafib (TNO155)
almost3years
New P3 trial • IO biomarker
|
EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1)
|
PD-L1 expression • EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
Imfinzi (durvalumab) • oleclumab (MEDI9447) • monalizumab (IPH2201)
almost3years
New P3 trial
|
EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
Imfinzi (durvalumab) • domvanalimab (AB154)
almost3years
SI-B001 Combined With Chemotherapy in the Treatment of EGFR/ALK WT Recurrent or Metastatic NSCLC. (clinicaltrials.gov)
P2/3, N=60, Recruiting, Sichuan Baili Pharmaceutical Co., Ltd. | Not yet recruiting --> Recruiting
Enrollment open • Combination therapy
|
EGFR (Epidermal growth factor receptor) • ALK (Anaplastic lymphoma kinase)
|
EGFR wild-type • ALK wild-type • EGFR wild-type + ALK wild-type
|
cisplatin • paclitaxel • docetaxel • pemetrexed • izalontamab (SI-B001)