Is NCT07157033 recruiting in Irvine, CA?

Yes, NCT07157033 is currently recruiting participants at its Irvine, CA location. This locally advanced pancreatic adenocarcinoma clinical trial is actively enrolling qualified participants.

Is participation in this Irvine clinical trial free?

Yes, all study-related care is provided at no cost to qualified participants. Many studies also offer compensation for time and travel expenses.

Locally Advanced Pancreatic Adenocarcinoma Clinical Trial in Irvine, CA

Q: How do I join the locally advanced pancreatic adenocarcinoma clinical trial in Irvine?

To join this clinical trial in Irvine, complete the eligibility form on this page. A study coordinator will contact you to discuss next steps and determine if you qualify.

Who Can Participate

Inclusion Criteria

Cytologic or biopsy confirmed adenocarcinoma of the pancreas

Disease deemed amenable to definitive treatment with SBRT by being:

Locally-advanced and/or technically unresectable, as determined by a specialist pancreaticobiliary surgeon and as part of a multidisciplinary team review including of multiphase cross-sectional imaging, demonstrating: i. Greater than 180-degree tumor involvement of the superior mesenteric artery (SMA) ii. Greater than 180-degree tumor involvement of the celiac axis including major branches of the celiac axis that would render the tumor unresectable (e.g. common hepatic artery) iii. Tumor involvement of the first branch of the SMA that is not surgically reconstructible iv. Long segment involvement of the superior mesenteric vein/portal vein/hepatic artery that is not amenable to surgical reconstructible.

Potentially resectable anatomically but deemed not a surgical candidate after multidisciplinary review (such as unresectable due to comorbid conditions that render. the risks of surgery prohibitive)

Potentially resectable but the patient elects to refuse surgery and prefers to pursue SBRT, and disease is deemed eligible for SBRT

Primary tumor involvement abutment of the bowel is allowed, however bowel infiltration or invasion (identified endoscopically or by contrast enhanced imaging) is not allowed.

No distant metastatic disease either prior to or following induction systemic therapy

Completion of medically indicated first line systemic therapy, which may include but is not limited to regimens such as FOLFIRNOX, gemcitabine/abraxane, and similar regimens

Patients must be able to understand and comply with any treatment related procedures for SBRT. including breath-hold techniques or tolerance of compression belt, or other motion management strategies for SBRT delivery.

Age 18 years or older

Eastern Cooperative Group (ECOG) performance status 0, 1, or 2

Adequate hematologic function as indicated by:

Absolute neutrophil counts \>/= 1500/mm3

Hemaglobin \>/= 8.0 g/dL

Plor current use of hepato atelet count \>/= 75,000/mm3

No known liver disease or hepatic impairment, as well as no recent or current use of hepatotoxic drugs or substances that could compromise liver function unless a washout period has been completed. Adequate liver function as indicated by:

Total bilirubin \</= 1.5x upper limits of normal (per institutional laboratory reference standard)

Aspartate aminotransferase (AST) and alanine aminotranferase (ALT) \</= 2.5 upper limits of normal (per institutional reference standard)

Baseline serum calcium level \>/= 8.4 mg/dL

No clinically significant history or presence of safety 12-lead ECG findings as judged by the investigator at screening and check-in(s), including each criterion as listed below:

Normal sinus rhythm (heart rate between 40 and 100 bpm)

QTcF interval \</= 470 msec

QRS interval \</= 110 msec

and PRS interval \</= 220 msec Repeat measurements may be performed at the discretion of the investigator or designee

An understanding, ability, and willingness to fully comply with the protocol-defined schedule of assessments, procedures, and restrictions

Must provide written informed consent prior to the initiation of any protocol specific procedures

The effects of XER-001 on the developing human fetus are unknown. For this reason women of child-bearing potential must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for at least six months following the last (fifth) day of radiotherapy on this study. Exceptions to this inclusion criterion are available to women who meet any of the following criteria:

Postmenopausal (no menses in greater than or equal to 12 consecutive months or validated by follicle stimulating hormone \[FSH\] levels.

History of hysterectomy or bilateral salpingo-oophorectomy

Ovarian failure (FSH and Estradiol in menopausal range, who have received Whole Pelvic Radiation Therapy)

History of bilateral tubal ligation or another surgical sterilization procedure

Approved methods of birth control are as follows: hormonal contraception (I.e. birth control pills, injection, implant, transdermal patch, vaginal ring), intrauterine device (IUD), tubal ligation or hysterectomy, subject/partner post vasectomy, implantable or injectable contraceptives, and condoms with spermacide. Not engaging in sexual activity through six months following the last (fifth) day of radiotherapy on this study is an acceptable practice; however periodic abstinence, the rhytm method, and the withdrawal method are not acceptable methods of birth control. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately. For male participants on this trial, contraception is required as above dusing the study and for at least three months following the last (fifth) day of radiotherapy on this study if the have partners who can become pregnant (woman of child-bearing potential). Similarly, male participants on this trial should not donate sperm during the study and for at lease three months following the last (fifth) day of radiotherapy on this study.

Exclusion Criteria

Prior radiotherapy to the upper abdomen with overlap of. the anticipated SBRT field

Prior radiopharmaceutical therapy

Prior surgical resection of the pancreatic tumor

Uncontrolled or active gastric or duodenal ulcer disease within 30 days of enrollment

Visable invasion of tumor into the bowel/stomach.duodenal lumen on endoscopic evaluation

Residual or ongoing grade 3+ non-hemotological toxicity from chemotherapy other than alopecia

Concurrent participation in another interventional clinical trial or use of another investigational agent within 30 days of study consent. Note that participation in non-interventional clinical trials (e.g. quality of life \[QOL\], imaging, etc) is not exclusionary

Uncontrolled intercurrent illness including but not limited to: ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, renal failure, cardiac arrhythmia

Patients with history of myocardial infarction or unstable angina within 6 months prior to study enrollment

Patients with history of symptomatic or (CTCAE-defined) grade 3+ hypocalcemia

Patients with history of hypoparathyroidism

Patients with history of hypertension where medical providers deem that interruption of antihypertensive regimen for one week is deemed unsafe.

Patients with systolic blood pressure (BP) \< 100 or diastolic BP \< 65 at screening or baseline

History or presence of a disease, such as hepatic impairment or renal insufficiency, that could affect the absorption, distribution, metabolism, or elimination of the investigational product, tolerance to radiotherapy, or could affect clinical or laboratory assessments. Patients with an estimated glomerular filtration rate of less than 30 mL per minute are excluded from the trial. Patients with total bilirubin greater than 2.5 mg/dL are excluded from the trial unless patient has history of Gilbert's syndrome. In case of suspected or confirmed Gilbert's syndrome, bilirubin will be fractionated, and patients with direct bilirubin greater than 1.5 mg/dL will be excluded from the trial.

History of cardiac-related condition, which may include, but is not limited to, torsades de pointes, ventricular fibrillation, or ventricular tachycardia

Presence or family history (parents and siblings) of congenital lqt syndrome or any premature history of myocardial infarction considered clinically significant by the investigator or designee

History or presence of palpitations, unexplained syncope, shortness of breath or any other symptoms that may relate to cardiac arrhythmias

Any ECG evidence of physiological variants predisposing to electrical instability (eg. frequent pre-ventricular systolic beats)

Medical disorder that may require treatment during the study or make the subject unlikely to complete the study.

Inability to fast for 3 hours prior to study drug administration

Known history of active hepatitis B/C or active human immunodeficiency virus (HIV) not on highly-active anti-retroviral therapy for a minimum of 30 days

Donation or loss of more than 500 ml of whole blood within 30 days prior to screening

Difficulty with venous access or unstable or unwilling to undergo catheter insertion

Female subjects who are currently pregnant (have a positive pregnancy test), are lactating, or planning to breastfeed. Pregnant or breastfeeding women are excluded from this study because there is an unknown risk for adverse events in nursing infants secondary to treatment of the mother with amifostine, breastfeeding should be discontinued if the mother is treated with amifostine

An employee of the sponsor or research site personnel directly affiliated with this study or their immediate family member defined as a spouse, parent, child, or sibling, whether biological or legally adopted

A subject who, in the opinion of the investigator or designee, is considered unsuitable or unlikely to comply with the study protocol for any reason

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Irvine?

Yes, this clinical trial (NCT07157033) has an active research site in Irvine, CA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Locally Advanced Pancreatic Adenocarcinoma Treatment Options in Irvine, CA

If you're searching for locally advanced pancreatic adenocarcinoma treatment options in Irvine, CA, this clinical trial (NCT07157033) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Irvine research site is actively enrolling participants for this clinical trial. You'll receive care from experienced locally advanced pancreatic adenocarcinoma specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all locally advanced pancreatic adenocarcinoma clinical trials near you to find additional studies recruiting in your area.

Locally Advanced Pancreatic Adenocarcinoma Clinical Trial in Irvine, CA

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