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A Phase I open label, dose-escalation and expansion study to evaluate the safety, tolerability, pharmacokinetics and preliminary efficacy of AK135 for the treatment of chemotherapy-induced peripheral neuropathy in patients with malignant tumor
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| AK135 | Experimental | Each subject will receive a single dose of AK135 every 2-week cycle (Q2W) or every 1-week cycle (QW) or every 3-week cycle (Q3W). |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| AK135 | Drug | IV infusion, specified dose with specified treatment frequency |
|
| Measure | Description | Time Frame |
|---|---|---|
| Adverse events | Incidence and severity of participants with adverse events | From time ICF is signed until 90 days after last dose of AK135 |
| DLT | During the first treatment cycle of AK135 (14 days) |
| Measure | Description | Time Frame |
|---|---|---|
| EORTC-QLQ-CIPN20 | Patient-assessed European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-CIPN twenty-item scale | through study completion, an average of 12 weeks |
| BPI-SF |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Xufang Yu | Contact | +86(0760)8987399 | clinicaltrials@akesobio.com |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Sun Yat-sen Memorial Hospital | Guangzhou | China |
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Patient-assessed Brief Pain Inventory-Short Form
| through study completion, an average of 12 weeks |
| CTCAE-Neuropathy | Physician-assessed Common Terminology Criteria for Adverse Events-Neurotoxicity | through study completion, an average of 12 weeks |
| Cmax of AK135 | through study completion, an average of 12 weeks |
| AUC | through study completion, an average of 12 weeks |
| t1/2 | through study completion, an average of 12 weeks |
| ADAs | Number of subjects who develop detectable anti-drug antibodies | From first dose of study drug through 30 days after last dose of study drug. |
| Shanghai GoBroad Cancer Hospital | Shanghai | China |