New combo therapy targets Stomach-Lining cancer in early trial
NCT ID NCT07454031
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early-phase study tests a new drug combination (PX plus nab-paclitaxel) given directly into the abdomen for people with a type of advanced cancer that has spread to the lining of the belly. The main goal is to find a safe dose and check for side effects. About 22 adults with this specific cancer will take part.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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About 22 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Mar 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age ≥ 18 years, regardless of sex; * Histologically confirmed peritoneal metastatic mucinous adenocarcinoma; * Considered suitable for intraperitoneal therapy based on investigator assessment; * ECOG performance status 0-2; * Adequate organ function confirmed by laboratory tests within 7 days prior to enrollment: * Hematology: ANC ≥ 1.5 × 10⁹/L; PLT ≥ 100 × 10⁹/L; Hb ≥ 85 g/L; Liver function: TBIL ≤ 1.5 × ULN (≤ 3 × ULN for Gilbert's syndrome);AST/ALT ≤ 3 × ULN (≤ 5 × ULN in patients with liver metastases); Renal function: creatinine clearance ≥ 60 mL/min (Cockcroft-Gault) or serum creatinine ≤ 1.5 × ULN; Coagulation: PT, INR, and APTT ≤ 1.5 × ULN; * Life expectancy ≥ 3 months; * Ability to understand and willingness to sign written informed consent. Exclusion Criteria: * Planned concomitant systemic anti-tumor therapy during intraperitoneal treatment; * Massive ascites not expected to be adequately drained prior to dosing; * Chemotherapy or radiotherapy within 4 weeks prior to enrollment (≥ 6 weeks for nitrosoureas or mitomycin C); * Pregnancy or lactation, or unwillingness to use effective contraception; * Severe abdominal infection or gastrointestinal obstruction; * Known peritoneal adhesions deemed unsuitable for catheter placement; * Active bleeding, uncorrected coagulation disorders, or inability to safely interrupt therapeutic anticoagulation; * Known hypersensitivity to PX, nab-paclitaxel, or excipients; * Pre-existing ≥ Grade 2 peripheral sensory neuropathy; * Severe or uncontrolled comorbidities that may increase study risk or interfere with evaluation; * Active or severe autoimmune disease, or ongoing systemic immunosuppressive therapy; * Positive for HBsAg, anti-HCV, syphilis antibody, or HIV antibody; * Psychiatric or cognitive disorders affecting compliance; * Any other condition deemed unsuitable by the investigator.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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