A randomized study to determine safety and efficacy of single subcutaneous (SC) administration of HAL treatment in patients with CINP.
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To explore the efficacy of Halneuron in the treatment of patients with Chemotherapy-Induced Neuropathic Pain
Timeframe: From enrollment to end of study at 4 weeks
To explore the Safety of Halneuron in the treatment of patients with Chemotherapy-Induced Neuropathic Pain
Timeframe: From enrollment to end of study at 4 weeks