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Antroquinonol for Metastatic Pancreatic Cancer
Phase 1 & 2
Waitlist Available
Research Sponsored by Golden Biotechnology Corporation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
No Placebo-Only Group
Summary
This trial tests a new drug, antroquinonol, combined with standard chemotherapy drugs to treat advanced pancreatic cancer. It aims to find the safest dose and see how well the combination works. The study focuses on patients who haven't been treated before for their cancer.
Who is the study for?
Adults over 18 with Stage IV metastatic pancreatic cancer, who haven't had systemic therapy for it (except certain past therapies if progression occurred >6 months ago). They must have a life expectancy of at least 12 weeks, be able to consent, and agree to use effective contraception. Excluded are those with uncontrolled illnesses or conditions that could affect safety or study compliance, known allergies to trial drugs, inability to take oral meds, recent substance abuse issues, other cancers within the last 5 years (with some exceptions), and active infections.
What is being tested?
The trial is testing Antroquinonol combined with standard chemotherapy drugs nab-paclitaxel and gemcitabine in patients newly diagnosed with metastatic pancreatic cancer. It's a two-part study: first determining the maximum tolerated dose of Antroquinonol (Phase I) and then assessing its effectiveness alongside standard treatment (Phase II).
What are the potential side effects?
Possible side effects include reactions related to the immune system due to Antroquinonol or chemotherapy agents like nab-paclitaxel and gemcitabine. These can range from mild allergic responses to severe organ inflammation. Other common chemo-related side effects may involve fatigue, digestive issues such as nausea or diarrhea, blood cell count changes leading to increased infection risk.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
MTD( phase I)
tumor assessment in millimeters
Secondary study objectives
Area Under the Curve
Body Surface Area in meter^2
CA-19-9 Antigen
+2 moreSide effects data
From 2018 Phase 2 trial • 31 Patients • NCT0204734497%
Gastrointestinal disorders
65%
General disorders and administration site conditions
55%
Respiratory, thoracic and mediastinal disorders
35%
Metabolism and nutrition disorders
35%
Nervous system disorders
26%
Musculoskeletal and connective tissue disorders
19%
Infections and infestations
19%
Investigations
13%
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
13%
Renal and urinary disorders
13%
Psychiatric disorders
6%
Cardiac disorders
6%
Tachycardia
100%
80%
60%
40%
20%
0%
Study treatment Arm
Antroquinonol (Hocena)
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Antroquinonol with SOCExperimental Treatment1 Intervention
Antroquinonol will first be conducted by dose escalation(200mg TID and 300mgTID) to characterize the safety of antroquinonol in combination with the standard of care (SOC) (nab-paclitaxel + gemcitabine) and to identify the MTD of antroquinonol in patients with metastatic pancreatic cancer.
At the cohort expansion part of the study, up to an additional 40 patients will be enrolled at the MTD or MFD/RD.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Antroquinonol
Not yet FDA approved
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for pancreatic cancer, such as gemcitabine and nab-paclitaxel, work by interfering with the DNA replication process, thereby inhibiting cancer cell proliferation and inducing apoptosis. Antroquinonol, currently under study, is believed to inhibit cancer cell growth and induce apoptosis through multiple pathways, including the inhibition of the PI3K/AKT/mTOR pathway, which is crucial for cell survival and proliferation.
Understanding these mechanisms is vital for pancreatic cancer patients as it helps in selecting targeted therapies that can effectively disrupt cancer cell growth and improve treatment outcomes.
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Who is running the clinical trial?
CovanceIndustry Sponsor
119 Previous Clinical Trials
12,766 Total Patients Enrolled
Golden Biotechnology CorporationLead Sponsor
11 Previous Clinical Trials
520 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My condition involves a tumor in the pancreas.I cannot take pills by mouth or have severe ongoing diarrhea.I haven't taken any strong medication affecting liver enzymes in the last 14 days.I am not pregnant, breastfeeding, and if capable of having children, I am using effective birth control.I have HIV, active hepatitis B, or active hepatitis C.I do not have any severe illnesses or social situations that would prevent me from following the study's requirements.You have a known or suspected problem with drugs or alcohol.I have not started any new cancer treatments recently.I do not have a serious infection requiring IV treatment.I haven't had any cancer except for certain skin, cervical, bladder, or early prostate cancers in the last 5 years.I am not allergic to nab-paclitaxel, gemcitabine, or antroquinonol.Your blood, liver, and kidney function tests must show that they are working properly. Your hemoglobin, white blood cell count, platelet count, liver enzymes, albumin, and kidney function need to be within certain ranges.My pancreatic cancer is confirmed and measurable.I am fully active or can carry out light work.Women who could become pregnant must have a negative pregnancy test before joining the study.I agree to use two effective birth control methods during and 3 months after the study.I have metastatic pancreatic cancer and haven't received systemic therapy, except possibly adjuvant or neoadjuvant therapy if my cancer progressed more than 6 months after the last treatment or surgery, and I have never had nab-paclitaxel.I am 18 years old or older.I was diagnosed with cancer that has spread within the last 6 weeks.The doctor thinks you will live for at least 12 more weeks.
Research Study Groups:
This trial has the following groups:- Group 1: Antroquinonol with SOC
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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