Minnelide™ Capsules with Paclitaxel for Advanced Gastric Cancer

A Phase 1 Open-Label, Dose-Escalation, Safety, Pharmacokinetic, and Pharmacodynamic Study of Minnelide™ Capsules Given Alone or in Combination With Paclitaxel in Patients With Advanced Gastric Cancer

This study is testing if Minnelide™ capsules, alone or with paclitaxel, can help people with advanced gastric cancer feel better and improve their chances of survival.

Quick facts

• Phase: Phase 1
• Study type: Interventional
• Enrollment: 36 (estimated)
• Ages: 19 Years and up
• Sex: All
• Sponsor: Minneamrita Therapeutics LLC (Industry-sponsored)
• Drugs / interventions: chemotherapy, radiation
• Locations: 1 site (Soeul)
• Trial ID: NCT05566834 on ClinicalTrials.gov

What this trial studies

This Phase 1 clinical trial evaluates the safety and effectiveness of Minnelide™ capsules, both alone and in combination with paclitaxel, in patients suffering from advanced gastric cancer. The study employs a dose-escalation approach to determine the optimal dosage while monitoring pharmacokinetics and pharmacodynamics. Previous research indicates that Minnelide™ may inhibit tumor progression and enhance survival rates in cancer patients. Participants will be closely monitored for any adverse effects and treatment responses.

Who should consider this trial

Good fit: Ideal candidates include adults aged 19 and older with histologically confirmed advanced gastric cancer that has progressed after standard chemotherapy.

Not a fit: Patients with early-stage gastric cancer or those who have not yet undergone standard chemotherapy may not benefit from this study.

Why it matters

Potential benefit: If successful, this treatment could provide a new therapeutic option for patients with advanced gastric cancer who have limited treatment alternatives.

How similar studies have performed: While this approach is novel in the context of advanced gastric cancer, similar studies using Minnelide™ in other cancer types have shown promising results.

Eligibility criteria

Inclusion Criteria:

* Patients with histologically confirmed advanced gastric cancer

  * Tumor progression after receiving standard/approved chemotherapy or where there is no approved therapy
  * One or more metastatic tumors measurable per RECIST v1.1 Criteria
  * Karnofsky performance ≥ 70%
  * Life expectancy of at least 3 months
  * Age ³ 19 years
  * Signed, written IRB-approved informed consent
  * A negative pregnancy test (if female)
  * Acceptable liver function:

    * Bilirubin 1.5 times upper limit of normal
    * AST (SGOT), ALT (SGPT) and Alkaline phosphatase 2.5 times upper limit of normal (if liver metastases are present, then 5 x ULN is allowed)
    * Albumin ≥ 3.0 g/dL
  * Acceptable renal function:

    o Serum creatinine within normal limits, OR calculated creatinine clearance ³ 60 mL/min/1.73 m2 for patients with creatinine levels above institutional normal.
  * Acceptable hematologic status:

    * Granulocyte

      * Monotherapy: ³ 1,500 cells/mm3
      * Combination therapy with paclitaxel: ³ 2,000cells/mm3 Platelet count ³ 100,000 (plt/mm3)
    * Hemoglobin ³ 9 g/dL
  * Urinalysis:

    o No clinically significant abnormalities
  * Acceptable coagulation status:

    * PT ≤ 1.5 times institutional ULN
    * PTT ≤ 1.5 times institutional ULN
  * Women of child- bearing potential and men must agree to use adequate contraception For men and women of child-producing potential, the use of effective contraceptive methods during the study and until 90 days after the last dose of IP for men or until 6 months after the last dose of IP for women or 6 months after the last dose of IP with paclitaxel for both men and women.

Exclusion Criteria:

New York Heart Association Class III or IV, cardiac disease, myocardial infarction within the past 6 months, unstable arrhythmia, or evidence of ischemia on ECG

* Baseline QTc exceeding 470 msec (using the Bazett's formula) and/or patients receiving class 1A or class III antiarrhythmic agents.
* Active, uncontrolled bacterial, viral, or fungal infections, requiring systemic therapy.
* Pregnant or nursing women. NOTE: For men and women of child-producing potential, the use of effective contraceptive methods during the study and until 90 days after the last dose of IP for men or until 6 months after the last dose of IP for women or 6 months after the last dose of IP with paclitaxel for both men and women. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.
* Treatment with radiation therapy (local therapy, non-target lesion, 2 weeks), major surgery, chemotherapy, biological agents or investigational therapy within 3 weeks prior to study treatment.
* Unwillingness or inability to comply with procedures required in this protocol
* Known infection with HIV, hepatitis B, or hepatitis C
* Serious nonmalignant disease (e.g., hydronephrosis, liver failure, or other conditions) that could compromise protocol objectives in the opinion of the investigator and/or the sponsor
* Patients who are currently receiving any other investigational agent
* Patients who are on a prohibited medication (section 4.3.2).
* Patients with biliary obstruction and/or biliary stent (Regimen B only)
* Patients with a history of severe hypersensitivity reactions to products containing Cremophor® EL (eg, cyclosporin for injection concentrate and teniposide for injection concentrate). • Patient with baseline ANC\<1500/mm3

Where this trial is running

Soeul

• Samsung Medical Center — Soeul, Korea, Republic of (Recruiting)

Study contacts

• Study coordinator: Mohana Velagapudi, MD

Conditions Gastric Cancer