New drug aims to stop chemo sickness in its tracks
NCT ID NCT07081256
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a new medicine called QLM2010 to see if it can prevent nausea and vomiting caused by strong chemotherapy. 665 adults with solid tumors who had never had chemo before took part. The goal was to see if QLM2010 works better than current standard drugs at stopping vomiting and the need for rescue medication.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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665 people
The number who actually took part.
- Started
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Jan 2025
- Finished
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Oct 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Able and willing to provide a written informed consent * 18 years of age or older, of either gender * Has a diagnosed malignant solid tumor through histological or cytological examination * Has never been treated with chemotherapy (Antitumor drugs are not used for cancer treatment, or intravesical instillation therapy for bladder cancer is not regarded as chemotherapy) * Receive the first course of cisplatin-based chemotherapy * Has a performance status (ECOG scale) of 0 to 2 * Predicted life expectancy of ≥ 3 months Exclusion Criteria: * .Subjects with poor blood pressure control after medication * Subjects with symptomatic brain metastases or any symptoms suggestive of brain metastasis or intracranial hypertension * Subjects with a history of severe cardiovascular diseases within 3 months prior to the administration of cisplatin, such as acute myocardial infarction, NYHA class II-IV heart failure, etc. * Subjects with a history of severe torsional ventricular tachycardia, QTcF\>480 ms * Subjects with mental disabilities or severe emotional or mental disorders, The investigators determined that inappropriate for participation in this clinical trial * Inadequate bone marrow, kidney, and liver function 10. Scheduled to receive any radiation therapy to the abdomen or pelvis from Day -7 through Day 6 * Scheduled to receive moderately or highly emetogenic chemotherapy from Day 2 through Day 6 * Subjects who have experienced emetic events (vomiting or dry vomiting) or nausea within 24 hours before cisplatin-based chemotherapy * Participated in clinical trials of other drugs within 30 days prior to the administration of cisplatin (received experimental drugs) * Subjects receiving palonosetron hydrochloride within 21 days before cisplatin-based chemotherapy. Subjects who previously received NK-1 receptor antagonists within 28 days prior to cisplatin-based chemotherapy. Subjects receiving glucocorticoid within 7 days before cisplatin-based chemotherapy. * Has taken the following agents within the last 48 hours 5-HT3 antagonists, Phenothiazines, Benzamides, Domperidone, Cannabinoids, Benzodiazepines, etc. * The investigators determined that other conditions were inappropriate for participation in this clinical trial
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Zhe jiangCancer Hospital
Hangzhou, China
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Other studies related to the condition(s) this trial covers.
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