Clinical trials: sponsored by LaNova Medicines Limited
Advanced Solid Tumor Cancer
A Phase I/II of LM-364 as a Single Agent or in Combination With Anti-tumor Therapy in Patients With Advanced Solid Tumors
For Phase I, to assess the safety and tolerability, obtain the recommended phase 2 dose (RP2D)/optimal biologic dose (OBD) and/or Maximum Tolerated Dose (MTD) for LM-364 as a single agent or in combination with tislelizumab in…
- Trial name
- LM364 (NCT07847905)
- Testing
- LM-364 for injection, Tislelizumab
- Where
- 8 sites in China
- Volunteers
- 90 people
- Sponsor
- LaNova Medicines Limited
Advanced Solid Tumor
A Study of LM-108 as Monotherapy or in Combination With Antitumor Therapies in Subjects With Advanced Solid Tumors
A Phase I/II, Open-Label, Dose-Escalation and Dose-Expansion Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Profile and Preliminary Efficacy of LM-108, an Anti-CCR8 Monoclonal Antibody, as Monotherapy or in…
- Trial name
- NCT05518045
- Testing
- LM-108, Toripalimab
- Where
- China
- Volunteers
- 392 people
- Sponsor
- LaNova Medicines Limited
Advanced Solid Tumor
A Phase I/II Study of LM-2417 in Subjects With Advanced Solid Tumours
This study is to assess the safety and tolerability, obtain the recommended phase 2 dose(RP2D)/or Maximum Tolerated Dose (MTD) for LM-2417 as a single agent or in combination with other anti-tumour agents in subjects with…
- Trial name
- NCT06682780
- Testing
- LM-2417, Docetaxel, Toripalimab/Tirelizumab
- Where
- China
- Volunteers
- 320 people
- Sponsor
- LaNova Medicines Limited
Advanced Solid Tumor
A Study of LM-168 Combined With Other Anti-tumor Treatments in Participants With Advanced Solid Tumors
For Safety introduction phase，this study is to evaluate the safety and tolerability of LM-168 in combination with other anti-tumor treatment regimens in participants of advanced solid tumor trials, determine the maximum tolerated…
- Trial name
- NCT07669415
- Testing
- LM-168, Tislelizumab, Docetaxel injection
- Where
- China
- Volunteers
- 108 people
- Sponsor
- LaNova Medicines Limited
Malignant Tumors
A Study of LM-364 as a Single Agent or in Combination With Anti-tumor Therapy in Patients With Advanced Solid Tumors
For Phase I, to assess the safety and tolerability, obtain the recommended phase 2 dose (RP2D)/optimal biologic dose (OBD) and/or Maximum Tolerated Dose (MTD) for LM-364 as a single agent or in combination with tislelizumab in…
- Trial name
- NCT07694765
- Testing
- LM-364 for injection, Tislelizumab
- Where
- 3 sites in Australia
- Volunteers
- 90 people
- Sponsor
- LaNova Medicines Limited
Locally Advanced or Metastatic GC and GCJ Adenocarcinoma
LM-108 in Combination With Toripalimab Versus Paclitaxel Injection for the Treatment of Subjects With CCR8-Positive Gastric and Gastroesophageal Junction Adenocarcinoma
This is a phase III， Multicenter, Randomized study， evaluating the efficacy and Safety of LM-108(an Anti-CCR8 mAb) in combination With Toripalimab Versus Paclitaxel Injection in subjects with CCR8-Positive locally advanced or…
- Trial name
- NCT07362186
- Testing
- LM-108 in combination with Toripalimab, Paclitaxel injection intravenous infusion
- Where
- China
- Volunteers
- 400 people
- Sponsor
- LaNova Medicines Limited
Advanced Solid Tumor Cancer
Phase II Study of LM-24C5
This study is to evaluate the efficacy and safety of the LM-24C5 in combination with other therapies in subjects with CEACAM5-positive advanced solid tumor
- Trial name
- NCT07387081
- Testing
- LM-24C5
- Where
- 2 sites in China
- Volunteers
- 130 people
- Sponsor
- LaNova Medicines Limited
Malignant Tumors
A Study of LM-350 in Subjects With Advanced Solid Tumours
For Phase I Dose Escalation Stage, to assess the safety and tolerability of LM-350 in patients with advanced solid tumors,determine the maximum tolerated dose (MTD) or optimal biological dose (OBD), and explore the relationship…
- Trial name
- NCT07112222
- Testing
- LM-350 for injection
- Where
- 4 sites in Australia, China
- Volunteers
- 80 people
- Sponsor
- LaNova Medicines Limited
Advanced Solid Tumours
A Study of LM-168 as a Single Agent or in Combination With Toripalimab in Subjects With Advanced Solid Tumours
For phase I ,this study is to assess the safety and tolerability, obtain the recommended phase 2 dose (RP2D) and/or Maximum Tolerated Dose (MTD) for LM-168 as a single agent or in combination with toripalimab in subjects with…
- Trial name
- NCT06868199
- Testing
- LM-168, Toripalimab
- Where
- 6 sites in Australia, China
- Volunteers
- 87 people
- Sponsor
- LaNova Medicines Limited
Advanced Solid Tumor
A Study of LM-24C5 For Advanced Solid Tumors
To assess the safety and tolerability, obtain the recommended phase 2 dose (RP2D)/optimal biologic dose (OBD) and/or Maximum Tolerated Dose (MTD) for LM-24C5 in subjects with advanced solid tumors.
- Trial name
- NCT06187402
- Testing
- LM-24C5
- Where
- 6 sites in United States
- Volunteers
- 49 people
- Sponsor
- LaNova Medicines Limited
Malignant Tumors
Study of LM-299 in Subjects Advanced Malignant Tumors
For Phase I Dose Escalation Stage, to assess the safety and tolerability of LM-299 in patients with advanced solid tumors,determine the maximum tolerated dose (MTD) or optimal biological dose (OBD), and explorethe recommended…
- Trial name
- NCT06650566
- Testing
- LM-299
- Where
- 6 sites in Australia, China
- Volunteers
- 108 people
- Sponsor
- LaNova Medicines Limited
Advanced Solid Tumor
A Study of LM-108 in Combination With Toripalimab in Subjects With Advanced Solid Tumours
Based on overall response rate (ORR) as assessed by the Independent Review Committee (IRC) against the Response Evaluation Criteria in Solid Tumors (RECIST v1.1) criteria for Solid Tumor Efficacy, To evaluate the efficacy of…
- Trial name
- NCT06873854
- Testing
- LM-108, Toripalimab
- Where
- China
- Volunteers
- 84 people
- Sponsor
- LaNova Medicines Limited
Malignant Tumors
A Phase I/II Study of LM-101 Injection in Patients With Advanced Malignant Tumors
This study is to assess the safety and tolerability, obtain Maximum Tolerated Dose (MTD) and/or the recommended phase 2 dose (RP2D) of LM-101 as a single agent or in combination in patients with advanced malignant tumors
- Trial name
- NCT05615974
- Testing
- LM101, Toripalimab, Rituximab
- Where
- 5 sites in China
- Volunteers
- 139 people
- Sponsor
- LaNova Medicines Limited
Relapsed or Refractory Multiple Myeloma, Other Plasma Cell Diseases
Study of LM-305 in Patients With Relapsed or Refractory Multiple Myeloma (RRMM) and Other Plasma Cell Diseases
A Phase I/II Study of LM-305 in Patients with Relapsed or Refractory Multiple Myeloma (RRMM)
- Trial name
- NCT05647512
- Testing
- LM-305, Dexamethasone
- Sponsor
- LaNova Medicines Limited
Advanced Solid Tumor
Study of LM-108 as a Single Agent or in Combination With Pembrolizumab in Subjects With Advanced Solid Tumours
A Phase I/II, Open-Label, Dose Escalation and Expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of LM-108 as a Single Agent or in Combination with Pembrolizumab in Advanced Solid…
- Trial name
- NCT05255484
- Testing
- LM-108, An Anti-PD-1 Antibody
- Where
- 6 sites in United States
- Volunteers
- 24 people
- Sponsor
- LaNova Medicines Limited
Advanced Tumours
Study of LM-061 in Subjects in Advanced Tumors
This is a phase I, open-label, dose escalation study to evaluate the safety, tolerability, PK, and preliminary efficacy of LM-061 in subjects with advanced tumors.
- Trial name
- NCT04737122
- Testing
- LM-061, Toripalimab
- Where
- Australia
- Volunteers
- 18 people
- Sponsor
- LaNova Medicines Limited
Advanced Tumours
A Clinical Study Preliminary Efficacy of LM-061 Tablet in Subjects With Advanced Tumours
This is a phase I/II, open-label, dose escalation and dose extension study to evaluate the safety, tolerability, PK, and preliminary efficacy of LM-061 in subjects with advanced tumors.
- Trial name
- NCT04882176
- Testing
- LM-061
- Where
- China
- Volunteers
- 18 people
- Sponsor
- LaNova Medicines Limited
Advanced Solid Tumors
Study of LM-102 in Subjects in Advanced Tumors
This is a phase Ⅰ, first-in-human, open-label, dose escalation study to evaluate the safety and tolerability, PK, immunogenicity and preliminary anti-tumor activity of LM-102 injection in subjects with CLDN18.2-positive advanced…
- Trial name
- NCT04735796
- Testing
- Drug：LM-102
- Where
- 6 sites in United States
- Volunteers
- 9 people
- Sponsor
- LaNova Medicines Limited