Phase Ⅰa Clinical Study of Hawthorn Red Pigment Combined... | NCT05561023

NCT05561023

Protocol Section

Identification Module

Results Section

No data available

No data is available for this block.

Annotation Section

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No data is available for this block.

Document Section

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Derived Section

Miscellaneous Info Module

Status Module

Design Module

Interventional Study Design

Biospecimen

No data available

No data is available for this block.

Arms/Interventions Module

Label	Type	Description	Intervention Names
Phase Ⅰ a clinical study	Other	"3 + 3" dose escalation scheme	Drug: Hawthorn red pigment

Interventions

Name	Type	Description	Arm Group Labels	Other Names
Hawthorn red pigment	Drug	For patients with refractory cancer pain who meet the enrollment conditions, on the basis of the clinician's normal adjustment of the analgesic regimen (the initial adjustment is the first day), the dose ramp up study of Hawthorn red pigment was started on the third day. The Hawthorn red dose group includes 10 tablets → 15 tablets → 20 tablets / time, orally, twice a day. "3 + 3" dose escalation scheme

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
AE, SAE and DLT, MTD (if any), RP2D	Occurrence and frequency of AE, SAE and DLT, MTD (if any), RP2D, Number of participants with treatment-related adverse events as assessed by CTCAE v4.0	1 month

Measure	Description	Time Frame
Average pain score	Change in average pain score (NRS 0-10, 0 = painless, 10 = most painful)	1 month

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

Patients aged 18-80 years with malignant tumor confirmed by pathology;
Refractory cancer pain, that is, patients coexist: 1) digital score of persistent pain ≥ 4 points and / or number of eruptive pain ≥ 3 times / day; 2) Following the relevant guidelines for cancer pain treatment, the pain relief of patients treated with opioids alone and / or combined with adjuvant analgesics for 1-2 weeks is still unsatisfactory and / or intolerable adverse reactions occur;
Patients who need chemotherapy, long-term hormone, targeted therapy or bisphosphate therapy had stable anti-tumor therapy before randomization;
Patients or their nursing staff can fill in the survey form;
Correctly understand and cooperate with medical staff in medication guidance;
No mental illness;
ECOG-ps ≤ 3 points; 8) Did not participate in the drug test (including the test drug) within one month before the test;
The subjects volunteered and signed the informed consent.

Exclusion Criteria:

patient is diagnosed with non cancerous pain or pain of unknown cause;
Postoperative pain of patients;
Patients with paralytic intestinal obstruction;
Patients with metastatic brain cancer;
Patients with opioid allergy / addiction;
Abnormal laboratory results with obvious clinical significance, such as creatinine ≥ upper limit of normal value, ALT or AST ≥ 2.5 times of upper limit of normal value (liver metastasis patients or primary liver cancer ≥ 5 times of upper limit of normal value), or child C level of liver function;
Patients who cannot take drugs orally;
Uncontrollable nausea and vomiting;
Patients with a history of gastritis and gastric ulcer;
Patients who need to use nonsteroidal drugs and steroid hormone drugs for analgesia;
Diabetes patients who can't control blood sugar stably;
Pregnant and lactating women; Subjects with pregnancy plans within 1 month after the trial (including male subjects);
Alcoholics;
Patients with cognitive impairment;
Patients with severe depression;
Diseases and conditions that other researchers consider not to be included.