A Study of the Safety and PK of PCS6422 (Eniluracil) with Capecitabine in Patients with Advanced, Refractory GI Tract Tumors

Phase 1

Completed

• Conditions: Advanced Cancer; Refractory Cancer; Tumor Gastric
• Interventions: Drug: PCS6422 and capecitabine

• Registration Number: NCT04861987
• Lead Sponsor: Processa Pharmaceuticals

Brief Summary

This study is an open label, multicenter study in patients who have advanced, relapsed refractory GI cancer or are not relapsed/refractory but are intolerant to other therapies who, in the judgment of investigators, are candidates for fluoropyrimidine monotherapy.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2021-04-23
• Study First Submitted QC: 2021-04-23
• Study First Posted: 2021-04-27
• Study Start: 2021-06-18
• Primary Completion: 2024-06-12
• Status Verified: 2024-09
• Study Completion: 2024-09-09
• Last Update Submitted: 2024-10-08
• Last Update Posted: 2024-10-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 23

Inclusion Criteria

1. Has advanced, metastatic or unresectable GI tract tumors that are refractory or intolerant to existing available therapies and for whom the investigator recommends fluoropyrimidine monotherapy.

2. Has measurable disease in accordance with Respond Evaluation Criteria in Solid Tumors (RECIST) guidelines (Version 1.1).

3. Is aged ≥18 years

4. Has not received treatment with intravenous (IV) 5 FU or oral 5 FU analogs in the 4 weeks preceding enrollment

5. Has Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-2 at study entry

6. Has adequate bone marrow, liver, and renal function as assessed by the following laboratory requirements conducted within 7 days before starting study treatment:

   1. peripheral ANC of ≥1.5 × 109/L
   2. platelet count of ≥75 × 109/L without growth factor/transfusion
   3. hemoglobin ≥8.5 g/dL without growth factor/transfusion
   4. estimated glomerular filtration rate >50 mL/min
   5. total bilirubin <2 × upper limit of normal (ULN); <5 × ULN if patient has liver metastases, biliary tract cancer; or ≤3 × ULN if the patient has Gilbert's disease
   6. Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) <2.5 × ULN, with liver metastasis <5 × ULN
   7. international normalized ratio (INR) <1.5

7. Has a life expectancy of at least 12 weeks

8. Female patients of childbearing potential and male patients with partners capable of reproduction must agree to use an effective contraceptive method from the time of Screening through 60 days after the last dose of capecitabine

9. Females of childbearing potential must have a negative serum β human chorionic gonadotropin pregnancy test result

10. Willingly provides written, informed consent.

11. Has resolution or stabilization of acute toxicity from prior therapy to Grade <2 - except Grade 2 neuropathy

12. If patient has human immune deficiency virus (HIV) infection, it is controlled with undetectable viral load with antiretroviral treatment.

13. If patient has hepatitis C infection and received antiviral treatment, has a negative viral load at Screening

14. If patient has chronic hepatitis B infection and is receiving antiviral treatment, has a negative viral load at Screening.

15. Is willing and able to comply with all protocol required visits and assessments

Exclusion Criteria

1. Is unable to take oral medication or malabsorption syndromes potentially interfering with medication absorption (e.g., short bowel syndrome or chronic, partial bowel obstruction)
2. Has history or presence of clinically significant abnormal 12 lead ECG results, in the investigator's opinion
3. Has current brain metastasis
4. Has prolonged QTc (with Fridericia's correction) of >480 msec in men and women performed at Screening
5. Has a history of prolonged QTc interval, ventricular tachycardia/fibrillation or significant ventricular arrhythmia, or Torsades de Pointes, or a history of ventricular ablation for arrhythmia
6. Has congenital long QT syndrome or a family history of long QT syndrome
7. Has other clinically significant cardiac disease including, but not limited to, uncontrolled angina, myocardial ischemia or infarction within 6 months, congestive heart failure >Class II per the New York Heart Association, or history of myocarditis
8. Has an electrolyte disturbance, such as uncorrected hypokalemia/hyperkalemia, hypomagnesemia, or hypocalcemia. Patients can be enrolled following successful correction of an electrolyte disturbance.
9. Is currently using any drugs included in the prohibited medications list in the protocol (including those that can prolong QTc) that cannot be discontinued
10. Has known hypersensitivity to any of the components of study treatments
11. Has other primary cancer requiring treatment within the last 3 years, except for cervical intraepithelial neoplasia, ductal carcinoma in situ, or completely excised squamous or basal cell carcinoma
12. Is a pregnant or lactating female
13. Had major surgery, open biopsy, or significant traumatic injury within 4 weeks prior to the first dose of study treatment
14. Is receiving or has received any investigational treatment within 4 weeks prior to study entry, or participating in another clinical study
15. Has known DPD deficiency

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
PCS6422 + Capecitabine	PCS6422 and capecitabine	Fixed dose of PCS6422 combined with various doses of Capecitabine administered in 14 day cycles

Primary Outcome Measures

Name	Time	Method
Number of participants with dose limiting toxicities (DLT) and incidence of adverse events as assessed by CTCAE v5.0	~6 months	Frequency, duration, and severity of DLTs and adverse events (AEs)
Maximum Plasma Concentration (Cmax) of capecitabine	~14 days	To evaluate the Maximum Plasma Concentration (Cmax) of capecitabine

Secondary Outcome Measures

Name	Time	Method
QTc effect of PCS6422	~6 months	To evaluate the effect of PCS6422 on QTc
Maximum Plasma Concentration (Cmax) of PCS6422	~14 days	To evaluate the Maximum Plasma Concentration (Cmax) of PCS6422
Number of participants with Adverse Events of Special Interest (AESI)	~6 months	Frequency, duration and severity of AESIs

Trial Locations

Locations (1)

Processa Clinical Site; 🇺🇸 Fairfax, Virginia, United States