Ulcerative Colitis
Conditions
Keywords
Ulcerative colitis, Inflammatory bowel disease, Interleukin 2, Interleukin-2, IL-2, Regulatory T Cells, Tregs, T-Lymphocytes, Regulatory
Brief summary
The purpose of this study is to determine the safety and maximum effective dose (MED) of Interleukin-2 in subjects with moderate-to-severe ulcerative colitis.
Detailed description
Interleukin-2 (IL-2) is a T cell growth factor. IL-2 is currently licensed for the treatment of metastatic renal cell carcinoma and metastatic melanoma, where it promotes the expansion of anti-cancer cytotoxic T cells and natural killer (NK) cells. However at low doses (100-times lower than those used in cancer therapy), IL-2 promotes the selective expansion of regulatory T cells (Tregs): an immune modulating subset of CD4+ lymphocytes. A recent phase 1 clinical trial from our collaborators at the Dana Farber Cancer Institute showed that low-dose IL-2 selectively expands Tregs in patients with treatment-resistant Graft vs. Host Disease (GvHD), and that low-dose IL-2 is safe in this condition. A detailed immunological analysis of samples from this study showed that low-dose IL-2 treatment was associated with increased Treg proliferation, increased de novo thymic generation of Tregs, and a resolution of defects in intracellular signalling and apoptosis seen in Tregs in chronic GvHD. A recent phase 1 study from another group showed that low-dose IL-2 is safe in the treatment of HCV-associated vasculitis. Low-dose IL-2 has also been shown to be well-tolerated in subjects with HIV. Ulcerative colitis (UC) is a chronic inflammatory disease of the colon. Evidence from pre-clinical models of intestinal inflammation, and also from patients with monogenetic defects in Treg function, suggests that Tregs play a role in the prevention of inflammation in the intestine. The treatment (or intervention) in this study is a once-daily, subcutaneous injection of IL-2, for a total of 8 weeks. The first 2 doses of the study drug will be administered by research nurses at Boston Children's Hospital. Further doses will be self-administered, at home. Training will be provided for correct self-administration. This is a 3+3 dose escalation study of IL-2 in moderate-to-severe UC. This study design is powered to identify the MED of low-dose IL-2 in UC. Once the MED is identified, a further 10 subjects will receive IL-2 at that dose. Recruitment of between 2 and 28 patients is planned. The maximum tolerated dose (MED) is the highest tolerated dose level at which a minimum of 6 subjects have been evaluated, with fewer than 2 evaluable subjects in 6 experiencing a dose limiting toxicity (DLT); i.e. DLT in \>1/6 evaluable subjects. In addition to the above at least 1 patient should meet the criteria for response or remission for it to be considered the MED. Dose levels are based on the experience of our collaborators in GvHD. In addition to determining the MED, this study will determine if low-dose IL-2 is safe and well-tolerated in patients with moderate-to-severe ulcerative colitis. A detailed immunological analysis of samples obtained from this study will determine if low-dose IL-2 expands Tregs in vivo, in patients with moderate-to-severe UC. Immunological changes will then be correlated with clinical response. The study will take place at Boston Children's Hospital. The study will involve 10 study visits. Most of the study visits involve blood tests. A flexible sigmoidoscopy or colonoscopy will be performed as part of the screening process. A flexible sigmoidoscopy will also be performed on completion of therapy, to determine clinical response. The first two subjects to receive the study drug will be admitted overnight following the first dose. Subsequent doses will be administered on an out-patient basis. All other subjects will receive IL-2 on an out-patient basis. Responders (with an acceptable side-effect profile) will be allowed to continue the study drug for at least 1 year. Compensation will be provided for participants.
Interventions
Description of intervention is covered in Arm, above.
Sponsors
Scott B. Snapper, MD PHD
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
* Age 18-70 years. * A diagnosis of UC made by standard clinical, radiological, endoscopic and histological criteria. * Moderate to severe UC with a Mayo score of 6-12. * Failure to tolerate or failure to respond to at least one conventional therapy with the intention of inducing or maintaining remission (examples include oral corticosteroids, oral 5-aminosalicylates, azathioprine and/or 6-mercaptopurine, or a tumor necrosis factor (TNF) antagonist). Corticosteroid dependency (inability to taper oral corticosteroids without a recurrence of disease activity) is also included in this category. * Stable doses of concomitant medications. * A negative pregnancy test in the 2 weeks prior to anticipated commencement of the study drug, in female subjects of child-bearing age. Men and women of reproductive potential must agree to use an acceptable method of birth control during treatment and for six months after completion of treatment. * Ability to provide informed consent.
Exclusion criteria
* A diagnosis of Crohn's disease or Inflammatory Bowel Disease - Unspecified (IBD-U, a diagnostic classification formerly termed indeterminate colitis). * Requirement for immediate surgical, endoscopic or radiological intervention for toxic megacolon, massive hemorrhage, perforation, sepsis, or intra-abdominal or perianal abscess. * Ileostomy, proctocolectomy or subtotal colectomy with ileorectal anastomosis. * History of colorectal cancer or dysplasia. * Positive stool test for Clostridium difficile. * Current medically significant infection. * Significant laboratory abnormalities, including; 1. Hb \< 8.0 g/dL, WBC \< 2.5 x 103/mm3, Plt \< 100 x 103/mm3. 2. Creatinine ≥ 1.5x institutional upper limit of normal (ULN). 3. Total bilirubin \> 2.0 mg/dL, ALT \> 2x institutional ULN, GGT \> 2x institutional ULN. Elevated unconjugated bilirubin related to Gilbert's syndrome is allowed. 4. Abnormal thyroid function tests. * Positive serology for HIV, hepatitis B virus (HBV) or HCV. * Positive screening test for tuberculosis (TB). * First dose of an anti-TNF medication within 4 weeks of anticipated study commencement, or a subsequent dose within 2 weeks of commencement; or ciclosporin or tacrolimus within 2 weeks of anticipated study commencement. * Received another investigational new drug (IND) within 5 half-lives of that agent before the planned commencement of SC IL-2. * Malignancy within the last 5 years. * Allergy to any component of the study drug. * Pregnant or lactating women. * Inability to comply with the study protocol or inability to give informed consent. * Prior exposure to IL-2. * Uncontrolled cardiac angina or symptomatic congestive cardiac failure (NYHA Class III or IV).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Subjects With Serious and Non-serious Adverse Events. | 8 weeks | Enumeration of the serious and non-serious adverse events seen in the study. Enumeration of any dose limiting toxicity seen in the study. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants With Clinical Response | 8 weeks. | A decrease from baseline in the total Mayo score of at least 3 points and at least 30% , with an accompanying decrease in the subscore for rectal bleeding of at least 1 point or an absolute subscore for rectal bleeding of 0 or 1 |
| Number of Participants With Clinical Remission | 8 Weeks | A total Mayo score of 2 points or lower, with no individual subscore exceeding 1 point |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Interleukin-2 Dose A Study drug: Interleukin-2 (aldesleukin, Proleukin, IL-2).
The dose levels will be as follows:
* Cohort 1: 0.3x10\^6 IU/m\^2/day. | 4 |
| Interleukin-2 Dose B \- Cohort 2: 1.0x10\^6 IU/m\^2/day. | 17 |
| Interleukin-2 Dose C \- Cohort 3: 1.5x10\^6 IU/m\^2/day | 5 |
| Total | 26 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 | FG002 |
|---|---|---|---|---|
| Overall Study | Adverse Event | 0 | 2 | 0 |
| Overall Study | Lack of Efficacy | 1 | 2 | 2 |
Baseline characteristics
| Characteristic | Interleukin-2 Dose B | Total | Interleukin-2 Dose A | Interleukin-2 Dose C |
|---|---|---|---|---|
| Age, Continuous | 43 years | 38.7 years | 36.7 years | 46.6 years |
| Extent Left-sided | 12 Participants | 17 Participants | 2 Participants | 3 Participants |
| Extent Pancolitis | 4 Participants | 7 Participants | 1 Participants | 2 Participants |
| Extent Ulcerative Proctitis | 1 Participants | 2 Participants | 1 Participants | 0 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 1 Participants | 1 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 16 Participants | 25 Participants | 4 Participants | 5 Participants |
| Region of Enrollment United States | 17 participants | 26 participants | 4 participants | 5 participants |
| Sex: Female, Male Female | 5 Participants | 8 Participants | 2 Participants | 1 Participants |
| Sex: Female, Male Male | 12 Participants | 18 Participants | 2 Participants | 4 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk |
|---|---|---|---|
| deaths Total, all-cause mortality | 0 / 4 | 0 / 17 | 0 / 5 |
| other Total, other adverse events | 4 / 4 | 17 / 17 | 5 / 5 |
| serious Total, serious adverse events | 0 / 4 | 0 / 17 | 0 / 5 |
Outcome results
Primary
Number of Subjects With Serious and Non-serious Adverse Events.
Enumeration of the serious and non-serious adverse events seen in the study. Enumeration of any dose limiting toxicity seen in the study.
Time frame: 8 weeks
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Interleukin-2 Dose A | Number of Subjects With Serious and Non-serious Adverse Events. | 0 Participants |
| Interleukin-2 Dose B | Number of Subjects With Serious and Non-serious Adverse Events. | 0 Participants |
| Interleukin-2 Dose C | Number of Subjects With Serious and Non-serious Adverse Events. | 0 Participants |
Secondary
Number of Participants With Clinical Remission
A total Mayo score of 2 points or lower, with no individual subscore exceeding 1 point
Time frame: 8 Weeks
| Arm | Measure | Category | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Interleukin-2 Dose A | Number of Participants With Clinical Remission | withdrew from trial | 1 Participants |
| Interleukin-2 Dose A | Number of Participants With Clinical Remission | Clinical Remission criteria not met | 3 Participants |
| Interleukin-2 Dose A | Number of Participants With Clinical Remission | Clinical Remission criteria met | 0 Participants |
| Interleukin-2 Dose B | Number of Participants With Clinical Remission | withdrew from trial | 4 Participants |
| Interleukin-2 Dose B | Number of Participants With Clinical Remission | Clinical Remission criteria met | 4 Participants |
| Interleukin-2 Dose B | Number of Participants With Clinical Remission | Clinical Remission criteria not met | 9 Participants |
| Interleukin-2 Dose C | Number of Participants With Clinical Remission | Clinical Remission criteria not met | 3 Participants |
| Interleukin-2 Dose C | Number of Participants With Clinical Remission | Clinical Remission criteria met | 0 Participants |
| Interleukin-2 Dose C | Number of Participants With Clinical Remission | withdrew from trial | 2 Participants |
Secondary
Number of Participants With Clinical Response
A decrease from baseline in the total Mayo score of at least 3 points and at least 30% , with an accompanying decrease in the subscore for rectal bleeding of at least 1 point or an absolute subscore for rectal bleeding of 0 or 1
Time frame: 8 weeks.
| Arm | Measure | Category | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Interleukin-2 Dose A | Number of Participants With Clinical Response | Clinical response criteria met | 1 Participants |
| Interleukin-2 Dose A | Number of Participants With Clinical Response | Clinical Response criteria not met | 2 Participants |
| Interleukin-2 Dose A | Number of Participants With Clinical Response | withdrew from trial | 1 Participants |
| Interleukin-2 Dose B | Number of Participants With Clinical Response | withdrew from trial | 3 Participants |
| Interleukin-2 Dose B | Number of Participants With Clinical Response | Clinical Response criteria not met | 5 Participants |
| Interleukin-2 Dose B | Number of Participants With Clinical Response | Clinical response criteria met | 9 Participants |
| Interleukin-2 Dose C | Number of Participants With Clinical Response | Clinical response criteria met | 0 Participants |
| Interleukin-2 Dose C | Number of Participants With Clinical Response | Clinical Response criteria not met | 3 Participants |
| Interleukin-2 Dose C | Number of Participants With Clinical Response | withdrew from trial | 2 Participants |