Offer your patients cutting-edge cancer treatment options
As a clinician, referring your patients to clinical trials can provide them with access to cutting-edge therapies that are not yet available in standard care. These trials are critical in evaluating the safety and efficacy of innovative treatments.
Participation in early phase trials has more potential for clinical benefit than is commonly believed, largely due to the development of modern cancer drugs, like targeted therapies, immunotherapies, and new combination therapies.
With internationally recognised Medical Directors, Professor Michael Millward and Professor Chan Cheah, overseeing Linear’s cancer clinical trials, there are multiple ways to partner with Linear to provide your patients access to clinical trials and engage seamlessly with the leading biopharmaceutical companies from around the world.
Refer a patient
Offer your patients cutting-edge cancer treatment options. Please see our referral form to start the process.
Supporting you in advancing cancer research and care
Diverse trial portfolio
Spanning a wide range of indications, our trials feature various innovative approaches, including immunotherapies, targeted treatments, combination regimens, and CAR-T cell therapy.
World-class facilities
Equipped with state-of-the-art technology and resources, the Advanced Clinical Trials Centre (ACTC) is able to admit eighteen participants with six overnight capabilities.
Dedicated investigator support
Full operational and regulatory support to streamline research and patient care.
Ready to make an impact as a trial investigator?
Becoming a principal investigator in phase 1 clinical trials opens a unique path to advancing both your career and the field of cancer. While Phase 1 trials may seem daunting due to administrative demands or safety concerns, our dedicated team is here to support you every step of the way. We handle the logistics, streamline processes, and maintain rigorous safety protocols, allowing you to focus on what matters most—leading impactful research that benefits patients and builds a legacy in cancer care.
Cancer trials currently running at Linear
Advanced Solid Tumours
AN8025S0101
A Phase I Open-label Study Evaluating the Safety, Pharmacokinetics, Pharmacodynamics, and Clinical Activity of AN8025 in Participants with Unresectable Advanced or Metastatic Solid Tumors
Advanced Solid Tumours
BG-89894-101
A Phase 1 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Antitumor Activity of BG-89894 (SYH2039) Tablets in Patients With Advanced Solid Tumors
Advanced Solid Tumours
MOMA-341-001
A Phase 1 Study of MOMA-341 as Monotherapy or Combination Therapy in Participants With Advanced or Metastatic Solid Tumors
Advanced Solid Tumors
OKN-4395-121
A Phase 1, Open-label, Multicenter, Dose-escalation and Cohort Expansion Study of OKN4395, a Triple Antagonist of EP2, EP4, and DP1 Prostanoid Receptors, as Monotherapy and in Combination With Pembrolizumab, in Patients With Advanced Solid Tumors
Advanced Ovarian Cancer
TORL123-002
Catalina-2: A Phase 2 Study Evaluating the Efficacy and Safety of TORL-1-23 in Women With Advanced Platinum-Resistant Epithelial Ovarian Cancer (Including Primary Peritoneal and Fallopian Tube Cancers) Expressing Claudin 6
Advanced Solid Tumors
SNV4818-101
A Phase 1, Open-Label Dose Escalation and Expansion Study of SNV4818 as Monotherapy or in Combination With Other Anticancer Agents in Participants With Advanced Solid Tumors
Advanced Solid Tumours
ADCE-T02-001
First-in-Human, Phase 1 Study of ADCE-T02, a Tissue Factor Targeted Antibody-Drug Conjugate, in Patients With Advanced Solid Tumors
Metastatic Castration-Resistant Prostate Cancer
HRS-5041-103
A Phase I, Open-label, Multi-Center, Non-Randomized Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of HRS-5041 in Subjects With Metastatic Castration-resistant Prostate Cancer
Advanced Solid Tumours
AP402-101
A Phase 1/2, Open-label Study of the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Clinical Activity of AP402 in HER2-Positive Patients with Locally or Advanced Solid Tumors
HR+/ HER2- Metastatic Breast Cancer
BGB-21447-102
A Phase 1 Study to Investigate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Antitumor Activity of BGB-21447 (a Bcl-2 Inhibitor) Combinations for Patients With HR+/HER2- Metastatic Breast Cancer
KRAS G12C Mutant Non-Small Cell Lung Cancer
TBBO8520-101
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
KRAS G12C Mutant Advanced Solid Tumours
FMC-376-CL101
An Open-Label, Phase 1/2 Dose Escalation, Dose Expansion and Cohort Expansion Study Evaluating the Safety, PK and Clinical Activity of FMC-376 in Participants With KRAS G12C Mutated Locally Advanced Unresectable or Metastatic Solid Tumors
Advanced Solid Tumours
VVD-159642-01
A Phase 1/1b, Open-label, Multicenter, First-in-Human Dose Escalation and Dose Expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Anti-tumor Activity of VVD-159642, a RAS-PI3Kα inhibitor, as a Single Agent and in Combination in Participants With Advanced Solid Tumors
Advanced Solid Tumours
GO43860
A Phase Ia/Ib, Open Label, Multicenter, Dose-escalation Study to Evaluate the Safety, Pharmacokinetics, and Activity of RO7502175 as a Single Agent and in Combination With Atezolizumab in Patients With Locally Advanced or Metastatic Solid Tumors
KRAS G12C-Mutant Advanced Solid Tumours
LOXO RAS-20001
A Phase 1a/1b Study of LY3537982 in Patients With KRAS G12C-Mutant Advanced Solid Tumors
Advanced Solid Tumours
BGB-A317-26808-101
A Phase 1 Study Investigating the Safety, Tolerability, Pharmacokinetics, and Preliminary Antitumor Activity of HPK1 Inhibitor BGB-26808 Alone or in Combination With Anti-PD-1 Monoclonal Antibody Tislelizumab in Patients With Advanced Solid Tumors
Advanced Squamous Non Small Cell Lung Cancer
HMBD-001-103
A Phase 1b study to evaluate HMBD-001 in combination with docetaxel with or without cetuximab in participants with advanced squamous non small cell lung cancer
Solid Tumors Harboring a TP53 Y220C Mutation
PMV-586-101
A Phase 1/2 Open-label, Multicenter Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of PC14586 in Patients with Locally Advanced or Metastatic Solid Tumors Harboring a TP53 Y220C Mutation (PYNNACLE)
Metastatic Triple-Negative Breast Cancer
CO42867
A Phase Ib/II, Open-Label, Multicenter, Randomized Umbrella Study Evaluating The Efficacy And Safety Of Multiple Immunotherapy-Based Treatment Combinations In Patients With Metastatic Triple-Negative Breast Cancer (Morpheus-TNBC)
Metastatic Castration-Resistant Prostate Cancer
PSMA-007-001
A Phase 1, Open-Label, Multicenter Study of JANX007 in Subjects With Metastatic Castration-Resistant Prostate Cancer
Advanced Solid Tumours
AXA-042-FIH-01
A Phase 1a/1b, first-in-human, open-label, non-randomized, multicenter, dose-escalation and dose-expansion study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of AXA-042 as monotherapy and in combination with checkpoint inhibitors in subjects with advanced solid tumors
Advanced Solid Tumours
IOS-1002-201
A Phase 1a/1b, First-in-human, Open-label, Non-randomized, Multicenter, Dose-escalation and Cohort Expansion Study to Evaluate the Safety, Tolerability, Efficacy, Immunogenicity, Pharmacokinetics, and Pharmacodynamics of IOS-1002 Administered Alone and in Combination With a PD-1 Monoclonal Antibody in Advanced Solid Tumors
Advanced Solid Tumours
BGB-A317-A3055-101
A Phase 1a/1b Study Investigating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Antitumor Activity of BGB-A3055, Alone and in Combination With Tislelizumab in Patients With Selected Advanced or Metastatic Solid Tumors
HER2 Expressing Advanced Solid Tumours
IKS014-01
An open-label, single-arm, Phase 1a/1b study with a 3+3 dose escalation phase, which evaluates FS-1502 (IKS014) in patients with HER2 expressing advanced solid tumors (Phase 1a) followed by an expansion cohort (EC) in HER2+ breast cancer (BCa) (Phase 1b)
KRAS G12D-Mutant Advanced Solid Tumours
INCB 161734-101
A phase 1, open-label, multicenter study of INCB161734 in participants with advanced or metastatic solid tumours with KRAS G12D mutation
Selected HER2 Expressing Tumours
DESTINY-PanTumor02
A Phase 2, Multicenter, Open-label Study to Evaluate the Efficacy and Safety of Trastuzumab Deruxtecan (T-DXd, DS-8201a) for the Treatment of Selected HER2 Expressing Tumors (DESTINY-PanTumor02)
BRAF and/or NRAS Mutation-positive Solid Tumours
KN-8701
A Phase 1/1b Open-label, Multicenter Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Antitumor Activity of KIN-2787 in Participants With BRAF and/or NRAS Mutation-positive Solid Tumors
Advanced Solid Tumours
D6900C00001
A Phase I/IIa Multi-center, Open-label Master Protocol to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Preliminary Antitumor Activity of AZD8205 in Participants with Advanced or Metastatic Solid Malignancies
Advanced Solid Tumours
DCSZ11-101
A Phase 1, Multicenter, Open-Label, Dose Escalation, and Dose Expansion Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Antitumor Activity of DCSZ11 as a Monotherapy in Patients with Advanced or Metastatic Solid Tumors
Advanced Solid Tumours
DB-1311-O-1001
A Phase 1/2a, Multicenter, Open-Label, First in Human Study to Assess the Safety, Tolerability, Pharmacokinetics, and Preliminary Antitumor Activity of DB-1311 in Subjects with Advanced/Metastatic Solid Tumors
Advanced or Metastatic Epithelial Tumours
MTX-TROP2-302
A Phase 1, Open-Label, First-in-Human, Dose Escalation Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of MT-302 in Adults With Advanced or Metastatic Epithelial Tumors
Mutant NF2 or mNF2 Advanced Solid Tumours
VT3989-001
Phase 1, Multi-Center, Open-Label Study of VT3989 in Patients with Refractory Locally Advanced or Metastatic Solid Tumors Enriched for Tumors Harboring Mutations of the Neurofibromatosis Type 2 Gene (mutant NF2 or mNF2)
Advanced Solid Tumours
GSK217228
A Phase 1 First-Time-in-Human, Open-Label Study of GSK4381562 Administered as Monotherapy and in Combination With Anticancer Agents in Participants With Selected Advanced Solid Tumors
Advanced Solid Tumours with MAPK Pathway Mutations
D3S-002-100
A Phase 1, Open-label, Dose-escalation Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Recommended Phase 2 Dose of D3S-002 Monotherapy in Adult Subjects with Advanced Solid Tumors with MAPK Pathway Mutations
Advanced Solid Tumors with a KRAS p.G12C Mutation
D3S-001-100
A Phase 1, Open-label, Dose-escalation and Dose-expansion Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of D3S-001 Monotherapy in Subjects with Advanced Solid Tumors with a KRAS p.G12C Mutation
Advanced Solid Tumours
BG-C9074-101
Phase 1a/1b Study of BG-C9074, an Antibody Drug Conjugate Targeting B7H4, as Monotherapy and in Combination With Tislelizumab in Participants With Advanced Solid Tumors
Advanced Solid Tumours with MTAP Deletion
BGB-58067-101
A Phase 1a/b Study Investigating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Antitumor Activity of BGB-58067, an MTA-Cooperative PRMT5
Advanced Solid Tumours GPC3-Expressing Cancers
MTX-GPC3-303
A Phase 1, Open-Label, First-in-Human, Dose Escalation Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of MT 303 in Adults with Advanced or Metastatic GPC3-Expressing Cancers, including Hepatocellular Carcinoma
Advanced Solid Tumours
PTT-4256-01
A Modular, Open Label, Dose Finding Phase 1/2 Clinical Trial in Patients with Solid Cancer to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of PTT-4256
Advanced Solid Tumours
BG-T187-101
A Phase 1 Study Investigating the Safety, Tolerability, Pharmacokinetics, and Preliminary Antitumor Activity of BG-T187, an EGFR×MET Trispecific Antibody, Alone and in Combination With Other Therapeutic Agents in Patients With Advanced Solid Tumors
Advanced Solid Tumours
AMT-676-01
First-in-Human, Phase 1 Study of AMT-676, an Anti-CDH17 Antibody-Drug Conjugate, in Patients with Advanced Solid Tumors
Advanced Solid Tumours with KRAS Mutation or Amplification
BGB-53038-101
A Phase 1a/1b Study to Investigate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Antitumor Activity of BGB-53038, a Pan-KRAS Inhibitor, as Monotherapy or in Combinations in Patients With Advanced or Metastatic Solid Tumors With KRAS Mutations or Amplification
Advanced Solid Tumours
SNV1521-101
A Phase 1, Open-Label Dose Escalation and Expansion Study of SNV1521 in Participants With Advanced Solid Tumors
Platinum-Resistant Ovarian, Peritoneal or Fallopian Tube Cancer
ZN-C3-002
A Phase 1b Study of ZN-c3 in Combination With Chemotherapy in Patients With Platinum-Resistant Ovarian, Peritoneal or Fallopian Tube Cancer
Advanced PRAME Positive Cancers
IMC-P115C-1005
A Phase 1 First-in-Human Study of the Safety and Efficacy of IMC-P115C as a Single Agent and in Combination with Standard of Care Agents in HLA-A*02:01 Positive Participants with Advanced PRAME Positive Cancers
Advanced Solid Tumours with a SMARCA4
PRT7732-01
A Phase 1 Open-Label, Multi-Center, Safety and Efficacy Study of PRT7732, an Oral SMARCA2 Degrader, in Patients with Advanced or Metastatic Solid Tumors with a SMARCA4
Advanced Solid Tumours
DB-1419-O-1001
A Phase 1/2a Multicenter, Open-Label, First in Human Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Antitumor Activity of DB-1419 in Subjects with Advanced/Metastatic Solid Tumors
Advanced Solid Tumours with AKT1 E17K Mutation
2618-001
AKTive-001: a Phase 1/1b Multiple Cohort Trial of ALTA2618 in Patients with Advanced Solid Tumors with AKT1 E17K Mutation
Ovarian, Endometrial, NSCLC
ZWI-ZW191-101
A Phase 1, Open-label, Multicenter Study to Assess the Safety, Tolerability, Pharmacokinetics, and Preliminary Anti-tumor Activity of Ascending Doses of a Folate Receptor Alpha Antibody Drug Conjugate, ZW191, in Participants with Advanced Solid Tumors
Advanced Urothelial Carcinoma or Other Solid Tumours
LOXO-LNC-24001
A Phase 1a/1b Study of LY4052031, a Nectin-4-targeted ADC, in Patients with Advanced or Metastatic Urothelial Carcinoma or Other Solid Tumors
T-Cell Lymphoma
CPI-818-004
A Phase 3, Randomized, Open-Label Study to Investigate the Efficacy and Safety of ITK Inhibitor Soquelitinib Versus Physician's Choice of Standard of Care Treatment (Selected Single Agent) in Participants with Relapsed/Refractory Peripheral T-cell Lymphoma Not Otherwise Specified, Follicular Helper T-cell Lymphomas, or Systemic Anaplastic Large-cell Lymphoma
Chronic Lymphocytic Leukemia, Small Lymphocytic Lymphoma
BGB-16673-304
A Phase 3, Open-Label, Randomized Study to Evaluate the Safety and Efficacy of BGB-16673 Compared to Pirtobrutinib in Patients With Relapsed/Refractory Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma
Mantle Cell Lymphoma
BGB-11417-302
A Phase 3 Randomized Double-Blind Multicenter Study of Sonrotoclax Plus Zanubrutinib Versus Placebo Plus Zanubrutinib in Patients With Relapsed/Refractory Mantle Cell Lymphoma
Cutaneous T-Cell Lymphoma
PTX-100-02-2024
An Open-Label, Phase 2 Study of PTX-100 Monotherapy in Patients With Relapsed or Refractory Cutaneous T-Cell Lymphoma.
Non-Hodgkin Lymphoma, Peripheral T-Cell Lymphoma
TLN-121-2501
An Open-Label, Multicenter, Phase 1 Trial to Evaluate the Safety, Pharmacokinetics, and Anti-Tumor Activity of TLN121 as a Single Agent and in Combination with Other Antilymphoma Agents, in Patients with Relapsed or Refractory Non-Hodgkin Lymphomas
Non-Hodgkin Lymphoma, Chronic Lymphocytic Leukemia
BGB-16673-101
A Phase 1, Open-Label, Dose-Escalation and -Expansion Study of the Bruton Tyrosine Kinase-Targeted Protein-Degrader BGB-16673 in Patients With B-Cell Malignancies
Waldenström Macroglobulinemia
BGB-11417-203
An Open-Label, Multicenter Phase 2 Study to Evaluate the Efficacy and Safety of the BCL2 Inhibitor Sonrotoclax (BGB-11417) as Monotherapy and in Combination with Zanubrutinib (BGB-3111) in Patients With Waldenström Macroglobulinemia
Non-Hodgkin Lymphoma
IKS03-01
A Phase 1 Cohort Dose Escalation and Expansion Trial to Determine the Safety, Tolerance, Maximum Tolerated Dose, and Preliminary Antineoplastic Activity of IKS03, a CD19-Targeting Antibody Drug Conjugate (ADC), in Patients with Advanced B cell Non-Hodgkin Lymphomas (NHL)
Non-Hodgkin Lymphoma, Chronic Lymphocytic Leukemia
BGB-21447-101
A Phase 1 Open-Label Dose-Escalation Study of Bcl-2 Inhibitor BGB-21447 in Patients With Mature B-Cell Malignancies
Non-Hodgkin Lymphoma, Chronic Lymphocytic Leukemia
DR-0201-ONC-001
A Multicenter, Multiple Expansion Cohort Phase 1 Study Evaluating the Safety and Activity of DR-0201 as Multiple Ascending Doses in Patients with Relapsed/Refractory B Cell Non-Hodgkin Lymphoma
Hodgkins Lymphoma
D9971C00001
A Modular Phase I/II, Open-label, Multicentre Study to Evaluate the Safety, Tolerability, and Efficacy of AZD3470, a PRMT5 Inhibitor, as Monotherapy and in Combination With Anticancer Agent(s) in Participants With Relapsed/Refractory Haematologic Malignancies
Multiple Myeloma
ISB 2001-101
A Phase 1, First-in-Human, Multicenter, Open-Label, Dose Escalation and Dose-Expansion Study of Single-Agent ISB 2001 in Subjects with Relapsed/Refractory Multiple Myeloma
Multiple Myeloma
D7230C00001
A Phase I/II, Open-Label, Multiple Centre Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Immunogenicity and Preliminary Efficacy of AZD0305 in Patients with Relapsed or Refractory Multiple Myeloma
Acute Myeloid Leukemia, Myelodysplastic Syndrome
BGB-11417-103
A Phase 1a/1b Open-Label Dose Escalation and Expansion Study of Bcl-2 Inhibitor BGB-11417 in Patients With Mature B-Cell Malignancies
Non-Hodgkin Lymphoma, Chronic Lymphocytic Leukemia
BGB-16673-104
A Phase 1b/2, Open-Label, Master Protocol Study of BTK-Degrader BGB-16673 in Combination With Other Agents in Patients With Relapsed or Refractory B-Cell Malignancies
FLT3 mutated AML
ZE46-0134-0002
A Phase 1, Open-label, Dose Escalation and Dose Expansion, Multicenter Clinical Trial to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of ZE46-0134 in Adults with FLT3 mutated Relapsed or Refractory Acute Myeloid Leukemia (AML)
Non-Hodgkin Lymphoma, Chronic Lymphocytic Leukemia
D9960C00001 (TITANium)
A Study to Evaluate Safety, PK, PD and Efficacy of AZD5492, a T Cell-engaging Antibody Targeting CD20 in Subjects With R/R B-Cell Malignancies (TITANium)
Chronic Lymphocytic Leukemia
BGB-11417-108
A Phase 1/2 Open-label Study to Investigate the Safety of Sonrotoclax Ramp-up Schedule(s) in Adult Patients With Hematological Malignancies.
Oncology Patient Referral Form