A Phase 2 interventional study of RRx-001 and Regorafenib in Colorectal Neoplasms, sponsored by EpicentRx, Inc.. Completed at 5 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-10-15.
Sponsored by EpicentRx, Inc. · Phase 2, Interventional, and Treatment
This two-stage study is designed to compare the safety and activity between RRx-001 against regorafenib followed by irinotecan-based therapies in a parallel comparative study.
Patients who are suffering from advanced or metastatic (meaning the disease has spread) colorectal cancer are invited to participate in this study. There will be two groups of patients (Randomized, open label study), one of these will receive RRx-001 and the other one will receive regorafenib. If patients qualify to participate in this study, they will be randomly assigned to the 'interventional arm' where patients will receive the experimental drug, RRx-001, or the 'control arm' where they will receive the current standard-of-care, Regorafenib. Patients have a 66% chance (2 out of 3) of receiving RRx-001 and a 33 % chance (1 out of 3) of receiving regorafenib.
On progression in the first part of the study, provided ECOG performance status is adequate, and if clinically appropriate i.e. there are no absolute or relative contraindications in the opinion of the Investigator, all subjects will enter the second part of the study and receive irinotecan plus bevacizumab.
Whether patients are given RRx-001 or regorafenib, they will also receive best supportive care, which includes treatments to help manage side effects and symptoms of cancer. This is an open label study, which means patients will know to which of these treatments, RRx-001 or regorafenib, they are assigned.
Purpose This two-stage study is designed to compare the safety and activity between RRx-001 against regorafenib followed by irinotecan-based therapies in a parallel comparative study.
Patients who are suffering from advanced or metastatic (meaning the disease has spread) colorectal cancer are invited to participate in this study. There will be two groups of patients (Randomized, open label study), one of these will receive RRx-001 and the other one will receive regorafenib. Qualifying patients will be randomly assigned (like the flip of a coin) to the 'interventional arm' and receive the experimental drug, RRx-001, or the 'control arm' where they will receive the current standard-of-care, Regorafenib. Patients will have a 66% chance (2 out of 3) of receiving RRx-001 and a 33 % chance (1 out of 3) of receiving regorafenib.
On progression in the first part of the study, provided ECOG performance status is adequate, and if clinically appropriate i.e. there are no absolute or relative contraindications in the opinion of the Investigator, all subjects will enter the second part of the study receive irinotecan plus bevacizumab.
Whether patients are given RRx-001 or regorafenib, they will also receive best supportive care, which includes treatments to help manage side effects and symptoms of cancer. This is an open label study, which means patients will know to which of these treatments, RRx-001 or regorafenib, they are assigned.
Background Oxygen is vital to life, we need it to breathe, for example, but at the same time it gives rise to byproducts that are toxic called free radicals. Free radicals are defined as "oxidants". Similarly, substances that interact with and neutralize free radicals, thus preventing them from causing damage, are called "antioxidants". Examples of recognizable antioxidants are Vitamin E, Vitamin C and beta-carotene. Antioxidants are also known as "free radical scavengers." When free radicals are present in excess of antioxidants damage may occur.
A free radical is an unstable molecule with an unpaired electron, an electrically charged particle, which seeks out another electron to return to a state of balance. An example of a free radical is hydrogen peroxide, recognizable as the household product that "bubbles" when it's poured on wounds. These bubbles come from oxygen free radicals, which are toxic to bacteria and all living cells, including cancer. The fact that these free radicals are toxic has to do with how reactive they are-imagine free radicals as high-speed ball bearings that smash into other molecules in order to "steal" back an electron and end their radical state, which sets off a chain reaction that transforms once stable compounds into a string of reactive radicals.
As new free radicals are created in this chain reaction, they randomly slam into whatever molecules they are closest to and steal their electrons, corroding them, like a biological form of rust. This process is repeated over and over, picking up speed, until an antioxidant can "neutralize" the free radicals and put a stop to the snowball effect. In the same way that this free radical bombardment can damage not only bacteria but also healthy tissues in the body, it is also capable of destroying cancer cells.
The current consensus is that compared to normal tissue tumor cells may accumulate elevated levels of free radicals, which contribute to the development of cancer. This is potentially a fatal weakness, a form of biological "Kryptonite", which can be used to advantage since the addition of even a small amount of free radicals may push the tumor over the edge, past the tipping point, above tolerable thresholds, breaking the camel's back. Similar to the expression "live by the sword, die by the sword", free radicals may lead to the development of cancer but they also are capable of harming it when present in excess.
RRx-001 is a completely new type of drug that comes from the U.S. aerospace or rocket science industry. It is activated to deliver free radicals to tissues that have low levels of oxygen. Compared to normal tissues, which have higher levels of oxygen, most, if not all, tumors exist in a low-oxygen environment, perhaps to prevent oxidation. In this way the free radicals delivered by RRx-001 to cancer cells under low oxygen conditions are able, in theory, to cause their targeted destruction without harming normal cells.
In general, colorectal tumors have low levels of antioxidants and, without this antioxidant protection, these tumors are more likely to be harmed by free radicals, so a treatment like RRx-001, which is able to increase the free radicals in the tumor, may benefit patients with colorectal cancer; this is a reason for studying RRx-001 in colorectal cancer. So far, in a Phase 1 study, 25 men and women with advanced, incurable cancer have received RRx-001 for different lengths of time and at doses that ranged from 10 mg/m2 to 83 mg/m2 once a week.
Regorafenib is a drug approved by the FDA to treat colon cancer after previous chemotherapy is no longer effective. It belongs to a class of targeted drugs known as tyrosine kinase inhibitors. Tyrosine kinases, which play a key role in many cell functions including cell growth and division, are commonly mutated or changed in cancer cells, becoming super-active and producing cells that have uncontrolled growth, and, therefore, blocking them with drugs like regorafenib may keep the cancer cells from growing.
5,738 studies on the registry are indexed under Colorectal Neoplasms; 1,481 are open to participants now.
This study's enrollment of 62 is below the median of 77 across 4,222 interventional studies indexed under Colorectal Neoplasms.
Browse Colorectal Neoplasms studies →EpicentRx, Inc. is the lead sponsor of 16 studies on the registry; none are open to participants now.
Of its 6 completed or terminated interventional studies of FDA-regulated products, 2 (33%) have results posted.
Counted across the registry records on this site, refreshed daily.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Once-weekly intravenous RRx-001 at a dose of 4 mg on Days 1, 8, 15, and 22 of a 4-week cycle. On progression and if eligible, patients will receive irinotecan (with or without bevacizumab)
Drug: RRx-001 · Drug: Irinotecan
Regorafenib daily on Days 1- 21 of a 4-week cycle. On progression and if eligible, patients will receive irinotecan (with or without bevacizumab)
Drug: Regorafenib · Drug: Irinotecan
Also known as: Stivarga
To be dosed after RRx-001 or regorafenib
Also known as: With or without bevacizumab
Overall Survival
From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 47 months
Time frame: From date of enrollment until death or censorship.
Progression Free Survival
Progression-free survival (PFS) will be defined as the elapsed time from the from date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 77 months
Time frame: Baseline, every 6-8 weeks while on study.
Number of Adverse Events
Incidence of related Adverse Events (AEs). SAEs and all other non-serious AEs are located in the Reported Adverse Event Module. National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) v4.03 is used to grade adverse events.
Time frame: Baseline through end of treatment (28 days after last dose of study drug). Approximately 24 weeks.
Objective Response Rate
Percentage of participants with ORR based assessment of confirmed complete response (CR) or confirmed partial response (PR) according to Response Evaluation Criteria in Solid Tumors (RECIST). CR was defined as complete disappearance of all target and non-target disease. PR applied only to participants with at least one measurable lesion. Greater than or equal to 30 % decrease under baseline of the sum of longest diameters of all target measurable lesions.
Time frame: Up to 2 years
Clinical Benefit Rate
The period from study entry through Disease Control. Disease Control Rate (DCR) also correlates to Clinical Benefit Rate (CBR), defined as the percentage of subjects with CR, PR or SD relative to the total number of treated subjects
Time frame: Up to 2 years
Participants were recruited based on physician referral at four academic medical centers between May 2014 and October 2019. The first participant first visit was May 22, 2014 and the last patient last visit was October 8, 2020.
| Milestone | RRx-001 Followed by Irinotecan | Regorafenib Followed by Irinotecan | Not Randomized |
|---|---|---|---|
| Started | 38 | 13 | 11 |
| Completed | 24 | 3 | 0 |
| Not completed | 14 | 10 | 11 |
| Withdrew: Physician decision | 4 | 5 | 0 |
| Withdrew: Withdrawal by subject | 3 | 1 | 0 |
| Withdrew: Adverse event | 7 | 4 | 0 |
| Withdrew: Ineligible | 0 | 0 | 11 |
From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 47 months
| months | RRx-001 Followed by Irinotecan | Regorafenib Followed by Irinotecan |
|---|---|---|
| Overall Survival | 8.6 (4.8 to NA) | 4.7 (2.2 to NA) |
Progression-free survival (PFS) will be defined as the elapsed time from the from date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 77 months
| months | RRx-001 Followed by Irinotecan | Regorafenib Followed by Irinotecan |
|---|---|---|
| Progression Free Survival | 6.1 (3.7 to NA) | 1.7 (0.7 to NA) |
Incidence of related Adverse Events (AEs). SAEs and all other non-serious AEs are located in the Reported Adverse Event Module. National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) v4.03 is used to grade adverse events.
| Number of total adverse events | RRx-001 Followed by Irinotecan | Regorafenib Followed by Irinotecan |
|---|---|---|
| CTCAE Grade 1 | 184 | 87 |
| CTCAE Grade 2 | 76 | 48 |
| CTCAE Grade 3 | 15 | 15 |
| CTCAE Grade 4 | 0 | 0 |
| CTCAE Grade 5 | 0 | 0 |
Percentage of participants with ORR based assessment of confirmed complete response (CR) or confirmed partial response (PR) according to Response Evaluation Criteria in Solid Tumors (RECIST). CR was defined as complete disappearance of all target and non-target disease. PR applied only to participants with at least one measurable lesion. Greater than or equal to 30 % decrease under baseline of the sum of longest diameters of all target measurable lesions.
| Participants | RRx-001 Followed by Irinotecan | Regorafenib Followed by Irinotecan |
|---|---|---|
| Partial Response | 5 | 0 |
| Stable Disease | 12 | 4 |
| Progressive Disease | 6 | 6 |
| Non-Evaluable | 1 | 0 |
The period from study entry through Disease Control. Disease Control Rate (DCR) also correlates to Clinical Benefit Rate (CBR), defined as the percentage of subjects with CR, PR or SD relative to the total number of treated subjects
| Participants | RRx-001 Followed by Irinotecan | Regorafenib Followed by Irinotecan |
|---|---|---|
| Clinical Benefit Rate | 17 | 4 |
Collected over Serious Adverse Events and **Other (Not Including Serious) Adverse Events** were collected beginning at baseline through end of treatment (28 days after last dose of study drug). All-Cause Mortality was assessed up to 47 months". Non-serious events are listed at a 5% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| RRx-001 Followed by Irinotecan | 3/38 (7.9%) | 14/38 (36.8%) | 19/38 (50%) |
| Regorafenib Followed by Irinotecan | 1/13 (7.7%) | 7/13 (53.8%) | 10/13 (76.9%) |
| Event | RRx-001 Followed by Irinotecan | Regorafenib Followed by Irinotecan |
|---|---|---|
| Disease progressionGeneral disorders | 3/38 | 0/13 |
| AV MalformationsCongenital, familial and genetic disorders | 0/38 | 1/13 |
| Abdominal painGastrointestinal disorders | 1/38 | 1/13 |
| Abdominal Pain lowerGastrointestinal disorders | 0/38 | 1/13 |
| ConstipationGastrointestinal disorders | 0/38 | 1/13 |
| Lower Gastrointestinal haemorrhageGastrointestinal disorders | 0/38 | 1/13 |
| Flank painMusculoskeletal and connective tissue disorders | 0/38 | 1/13 |
| Mental status changesPsychiatric disorders | 1/38 | 1/13 |
| HydronephrosisRenal and urinary disorders | 0/38 | 1/13 |
| HaemoptysisRespiratory, thoracic and mediastinal disorders | 0/38 | 1/13 |
| Event | RRx-001 Followed by Irinotecan | Regorafenib Followed by Irinotecan |
|---|---|---|
| AnorexiaMetabolism and nutrition disorders | 0/38 | 9/13 |
| Pain in ExtremityMusculoskeletal and connective tissue disorders | 0/38 | 8/13 |
| ErythemaSkin and subcutaneous tissue disorders | 0/38 | 8/13 |
| FatigueGeneral disorders | 16/38 | 7/13 |
| Rash maculo-papularSkin and subcutaneous tissue disorders | 0/38 | 7/13 |
| Abdominal painGastrointestinal disorders | 9/38 | 6/13 |
| HeadacheNervous system disorders | 0/38 | 6/13 |
| Infusion related reactionInjury, poisoning and procedural complications | 13/38 | 0/13 |
| DiarrheaGastrointestinal disorders | 12/38 | 1/13 |
| HyperbilirubinaemiaHepatobiliary disorders | 0/38 | 4/13 |
| Age, Continuous(years) | RRx-001 Followed by Irinotecan | Regorafenib Followed by Irinotecan | Not Randomized | Total |
|---|---|---|---|---|
| Mean | 53.7 ± 10.41 | 61.2 ± 11.65 | 58.1 ± 10.25 | 56.4 ± 9.33 |
| Sex: Female, Male(Participants) | RRx-001 Followed by Irinotecan | Regorafenib Followed by Irinotecan | Not Randomized | Total |
|---|---|---|---|---|
| Female | 21 | 9 | 6 | 36 |
| Male | 17 | 4 | 5 | 26 |
| Race/Ethnicity, Customized(Participants) | RRx-001 Followed by Irinotecan | Regorafenib Followed by Irinotecan | Not Randomized | Total |
|---|---|---|---|---|
| White | 21 | 11 | 10 | 42 |
| Black or African American | 5 | 0 | 0 | 5 |
| Unknown | 1 | 0 | 1 | 2 |
| Asian | 11 | 1 | 0 | 12 |
| Native Hawaiian or Other Pacific Islander | 0 | 1 | 0 | 1 |
| Region of Enrollment(participants) | RRx-001 Followed by Irinotecan | Regorafenib Followed by Irinotecan | Not Randomized | Total |
|---|---|---|---|---|
| United States | 24 | 10 | 11 | 45 |
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Studies of the drug tested here: RRx-001
EpicentRx, Inc.