A Phase 1 interventional study of Hawthorn red pigment in Hawthorn Red Combined Refractory Cancer Pain, sponsored by Fujian Cancer Hospital. Status unknown. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2022-09-30.
Sponsored by Fujian Cancer Hospital · Phase 1, Interventional, and Treatment
To evaluate the safety and tolerance of Hawthorn red pigment in the treatment of cancer pain
Determine the maximum tolerated dose (MTD, if any) of Hawthorn red pigment and the recommended dose for phase II clinical study (RP2D)
338 studies on the registry are indexed under Cancer Pain; 71 are open to participants now.
This study's planned enrollment of 14 is below the median of 60 across 254 interventional studies indexed under Cancer Pain.
Browse Cancer Pain studies →Fujian Cancer Hospital is the lead sponsor of 155 studies on the registry; 90 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
"3 + 3" dose escalation scheme
Drug: Hawthorn red pigment
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
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
Time frame: 1 month
Average pain score
Change in average pain score (NRS 0-10, 0 = painless, 10 = most painful)
Time frame: 1 month
No study locations are listed for this record.
This study is status unknown, as verified in Sep 2022. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
Fujian Cancer Hospital