이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

A Safety Trial to Evaluate an Orally Ingested Yeast Modified to Express a Tetra-specific Anti-toxin for Clostridioides Difficile

A Phase 1 Trial to Evaluate an Orally Ingested Probiotic Yeast Genetically Modified to Express a Tetra-specific Anti-toxin for Clostridioides Difficile

This is a Phase 1, first-in-human, double-blind, placebo-controlled, adaptive-design, single-site study, involving dose exploration cohorts.

During Part A, up to 4 cohorts, each consisting of approximately 14 healthy adult study participants, will be randomly allocated to receive either FZ002 or placebo. Part A is designed to begin with Cohort 1 evaluating the highest proposed dose of study product. This is intended to represent the "ceiling" (highest level) of the ranges of doses to be evaluated in the study. In the event of a safety or tolerability concern in Cohort 1, a dose de-escalation will be evaluated in Cohorts 2-4 until a safe and well-tolerated dose is identified. If no safety or tolerability concerns are identified at the completion of a cohort, the study will proceed to Part B with the approval of the independent Safety Monitoring Committee (SMC). This adaptive design allows for the progression of the study from Part A to Part B without necessarily progressing through all 4 cohorts in Part A if there is a lack of safety or tolerability concerns.

During Part B, an initial 'sentinel' Cohort 5 "some-risk" adult study participants will be randomly allocated to receive a single daily dose of FZ002 or placebo for 28 consecutive days. This is intended to represent the "floor" (lowest level) of doses to be evaluated in the study. A Protocol Safety Review Team (PSRT) will review the available safety data from the first 7 days of Cohort 5. If there is a lack of safety or tolerability concerns over the first 7-days of dosing for Cohort 5, then Cohort 6 will be opened for enrollment. Cohort 6 "some-risk" adult study participants will evaluate the "floor" and "ceiling" dose of FZ002 versus placebo.

The primary objective is to evaluate safety and clinical tolerability of oral doses of FZ002 or placebo when taken for up to 28 days.

연구 개요

상세 설명

This is a Phase 1, first-in-human, double-blind, placebo-controlled, adaptive-design, single-site study, involving dose exploration cohorts.

During Part A, up to 4 cohorts, each consisting of approximately 14 healthy adult study participants, will be randomly allocated to receive either FZ002 or placebo. Part A is designed to begin with Cohort 1 evaluating the highest proposed dose of study product. This is intended to represent the "ceiling" (highest level) of the ranges of doses to be evaluated in the study. In the event of a safety or tolerability concern in Cohort 1, a dose de-escalation will be evaluated in Cohorts 2-4 until a safe and well-tolerated dose is identified. If no safety or tolerability concerns are identified at the completion of a cohort, the study will proceed to Part B with the approval of the independent Safety Monitoring Committee (SMC). This adaptive design allows for the progression of the study from Part A to Part B without necessarily progressing through all 4 cohorts in Part A if there is a lack of safety or tolerability concerns.

During Part B, an initial 'sentinel' Cohort 5 "some-risk" adult study participants will be randomly allocated to receive a single daily dose of FZ002 or placebo for 28 consecutive days. This is intended to represent the "floor" (lowest level) of doses to be evaluated in the study. A Protocol Safety Review Team (PSRT) will review the available safety data from the first 7 days of Cohort 5. If there is a lack of safety or tolerability concerns over the first 7-days of dosing for Cohort 5, then Cohort 6 will be opened for enrollment. Cohort 6 "some-risk" adult study participants will evaluate the "floor" and "ceiling" dose of FZ002 versus placebo.

The primary objective is to evaluate safety and clinical tolerability of oral doses of FZ002 or placebo when taken for up to 28 days. The secondary objective is to evaluate laboratory abnormalities with FZ002 or placebo when taken for up to 28 days.

연구 유형

중재적

등록 (추정된)

86

단계

  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

설명

Inclusion Criteria:

To be eligible to participate in Part A of this trial, an individual must meet all of the following criteria:

  1. Provides written informed consent prior to the initiation of any trial procedures.
  2. Is able to understand and agrees to comply with all planned trial procedures and be available for all study visits, including:

    1. Receiving 28 days of blinded oral study product
    2. Providing blood and self-collected stool samples
  3. Is a non-pregnant individual, aged 18-75 years, inclusive, at the time of enrollment.
  4. Has no more than 1 single Grade 1 screening laboratory abnormality that is not clinically significant. If the participant has more than 1 Grade 1 abnormality, it must be approved by the Division of Microbiology and Infectious Diseases [DMID] Medical Monitor (MM).
  5. Participants of childbearing potential: use of adequate contraception for at least 4 weeks prior to enrollment and agreement to use such a method during trial participation and for an additional 4 weeks after the last dose of blinded study product. Note: Definitions of participants of childbearing potential and adequate contraception are provided in Section 13.1.
  6. Agrees to refrain from ingestion of probiotics* or fermented foods** from 7 days prior to study product administration, while on blinded study product, and through Day 36 (Visit 6).

    *E.g., probiotic nutritional Lactobacillus or Bifidobacterium supplements, yogurt, kefir, any "live and active culture" nutritional product, etc.

    **E.g., kombucha, fermented pickled vegetables, etc.

  7. Has good health by medical history, vital signs, physical examination, and concomitant medication review*. Participants should be stable based on their condition over the last 3 months prior to enrollment.

    *As defined by not requiring a change in therapy (including dose or frequency) or medical care for worsening disease for at least 3 months prior to enrollment. Vital signs must not meet Grade 1 or higher.

  8. Not using medications daily that may affect gut motility, gastric acidity, or baseline gut function* within 3 months of enrollment and through Day 36 (Visit 6).

    *E.g., proton pump inhibitors, opioids, anti-diarrheal agents, anti-constipation agents, daily Over-the-counter [OTC] "heartburn" relief medications.

  9. Not using glucagon-like peptide-1 (GLP-1) receptor agonists within 6 weeks of enrollment.
  10. Any elective surgery (including dental) that required preoperative or postoperative antibiotics must have been completed at least 3 months prior to enrollment.
  11. No history of Clostridioides difficile infection [CDI] (suspected or proven), no recent hospital admissions (within 3 years), and no receipt of systemic antibiotics known to increase risk of CDI* (within 6 months).

    *Systemic antibiotics that are known to increase the risk of CDI include lincosamides (e.g., clindamycin), monobactams (e.g., aztreonam), extended-spectrum penicillin combinations with beta-lactamase inhibitors (e.g., piperacillin-tazobactam), carbapenems (e.g., imipenem, meropenem, ertapenem), third generation or higher cephalosporins, and fluoroquinolones. Common oral antibiotics that would be allowable or are not known to significantly increase risk of CDI include amoxicillin, azithromycin, cephalexin, doxycycline, metronidazole, and trimethoprim/sulfamethoxazole.

  12. No history of other enteric infections or diarrheal illness within 3 months of enrollment.

In order to be eligible to participate in Part B of this trial, an individual must meet all of the following criteria:

  1. Provides written informed consent prior to the initiation of any trial procedures.
  2. Is able to understand and agrees to comply with all planned trial procedures and be available for all study visits, including:

    1. Receiving 28 days of blinded oral study product
    2. Providing blood and self-collected stool samples
  3. Is non-pregnant individual, aged 18-75 years, inclusive, at the time of enrollment.
  4. Has no more than 1 single Grade 1 hematology result and no more than 1 Grade 1 metabolic panel result. If the participant has more than 1 Grade 1 abnormality, it must be approved by the MM.
  5. Participants of childbearing potential: use of adequate contraception for at least 4 weeks prior to enrollment through 4 weeks after the last dose of blinded study product. Note: Definitions of participants of childbearing potential and adequate contraception are provided in Section 13.1.
  6. To rule out live microbial products and factors that may actively modulate the gut microbiome, participant agrees to refrain from ingestion of probiotics* or fermented foods** from 7 days prior to study product administration, while on blinded study product, and through Day 36 (Visit 6).

    * E.g., probiotic nutritional Lactobacillus or Bifidobacterium supplements, yogurt, kefir, any "live and active culture" nutritional product, etc.

    ** E.g., kombucha, fermented pickled vegetables, etc.

  7. Stable health by medical history, vital signs, physical examination, concomitant medication review, not requiring a change in therapy or medical care for worsening disease within 1 month of enrollment.
  8. Not using medications daily that may affect gut motility, gastric acidity, or baseline gut function* within 1 month of enrollment.

    *E.g., proton pump inhibitors, opioids, anti-diarrheal agents, anti-constipation agents, daily OTC "heartburn" relief medications.

  9. Not using GLP-1 receptor agonists within 6 weeks of enrollment.
  10. Any elective surgery (including dental) that required preoperative or postoperative antibiotics must have been completed at least 1 month prior to enrollment.
  11. Must have had at least 1 of these 3 conditions:

    1. History of CDI (suspected or proven) within the past 3 years, with "cure" or no symptoms for at least 1 month prior to enrollment
    2. History of a hospitalization within the past 3 years, but discharge not sooner than 1 month prior to enrollment
    3. History of receiving systemic antibiotics known to increase the risk of CDI* within the past 3 years, but last dose not sooner than 1 month prior to enrollment *Systemic antibiotics that are known to increase risk of CDI include lincosamides (e.g., clindamycin), monobactams (e.g., aztreonam), extended-spectrum penicillin combinations with beta-lactamase inhibitors (e.g., piperacillin-tazobactam), carbapenems (e.g., imipenem, meropenem, ertapenem), third generation or higher cephalosporins, and fluoroquinolones. Common oral antibiotics that would be allowable or are not known to significantly increase the risk of CDI include amoxicillin, azithromycin, cephalexin, doxycycline, metronidazole, and trimethoprim/sulfamethoxazole.
  12. No history of other enteric infections or diarrheal illness within 1 month of enrollment.

Exclusion Criteria:

  1. Dwells in a long-term care or skilled nursing facility (living independently with limited nursing care is allowable).
  2. Known to be pregnant or has a positive pregnancy test at screening or enrollment.
  3. Currently breastfeeding a child.
  4. Known to have significant hypersensitivity to any components of the study product; including S. boulardii (or any S. boulardii-based nutritional supplement), hydroxypropyl methylcellulose, and Microcrystalline cellulose [MCC].

    Hydroxypropyl methylcellulose is the major component of the capsule shell and MCC is the placebo component.

  5. Known to have significant hypersensitivity to a first-line antifungal therapy (i.e., fluconazole or amphotericin B) against Saccharomyces.
  6. Known to be immunocompromised or have known or suspected congenital or acquired immunodeficiency, as determined by the investigator.
  7. Receipt of immunosuppressive therapy such as anti-cancer chemotherapy or radiation therapy within 3 years of enrollment.
  8. Receipt of chronic (>/=14 days) immunosuppressive corticosteroids at a dose of >/=20 mg prednisone daily or prednisone equivalent within 30 days of enrollment, including oral, parenteral, or high-dose inhaled* corticosteroids.

    *High-dose inhaled corticosteroid is defined as >800 mcg/day of beclomethasone dipropionate CFC or equivalent. Intra-articular, intranasal, and topical steroids are allowable.

  9. Active malignancy or history of malignancy in the past 3 years (non-melanoma, excised, cured skin cancers are allowed).
  10. History of or testing positive for human immunodeficiency virus (HIV), hepatitis B, or active hepatitis C at screening (positive hepatitis C antibody and detectable hepatitis C virus RNA).
  11. Anticipated or current receipt of kidney dialysis treatment.
  12. Concurrent, acutely life-threatening disease or condition, or any unstable medical history, as determined by the investigator.
  13. Significant chronic gastrointestinal [GI] condition(s) or disease*.

    *Includes diagnosis of inflammatory bowel disease or active Rome IV irritable bowel syndrome, poorly controlled Celiac disease, active gastroparesis, toxic megacolon, colostomy, intestinal resection (except uncomplicated appendectomy), ileus, short gut syndrome, or recent (within 6 months of enrollment) diverticular bleeding requiring surgical intervention or transfusion.

  14. Recent (within 6 months of enrollment) history of difficulty with swallowing food, liquids, or pills.
  15. Prosthetic heart valve or indwelling foreign structure within vascular supply (e.g., no central line or indwelling catheter) or known to have moderate to severe valvular disease.
  16. History of alcohol abuse or drug addiction within 5 years of enrollment or that might interfere with the ability to comply with trial procedures.
  17. Diagnosis of schizophrenia, bipolar disease, or other significant psychiatric disease in the opinion of the investigator that may interfere with or pose a problem with compliance with the study or the welfare of the participant.
  18. Presence of mild, acute, or self-limited condition, such as fever or cough or other symptoms of upper respiratory tract infection within 7 days prior to planned randomization.
  19. Any chronic illness that, in the opinion of the investigator, is at a stage where it might interfere with trial conduct or completion or participant safety.
  20. Identified as a study site or contract research organization employee or family member who is involved in the protocol and may have direct access to trial-related data.
  21. Participating in another clinical trial investigating a vaccine, drug, medical device, or medical procedure within 4 weeks of enrollment through the last visit of the study.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 순차적 할당
  • 마스킹: 삼루타

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Part A Cohort 1 Arm FZ002
Healthy adults administered 4 capsules of FZ002 orally QH12 for 28 days. N=12
A recombinant live biotherapeutic product (rLBP) for oral administration, bioengineered from the parental S. boulardii (Sb) strain to constitutively produce ABAB, an anti-toxin against TcdA and TcdB of CDiff, intended to reduce the risk of CDI recurrence.
위약 비교기: Part A Cohort 1 Arm Placebo
Healthy adults administered 4 capsules of placebo orally QH12 for 28 days. N=2
The placebo is a capsule filled with commercially sourced pharmaceutical-grade microcrystalline cellulose (MCC), an inert substance. No anticipated risk related to the study product.
실험적: Part A Cohort 2 Arm FZ002
Healthy adults administered 2 capsules of FZ002 orally QH12 for 28 days. N=12
A recombinant live biotherapeutic product (rLBP) for oral administration, bioengineered from the parental S. boulardii (Sb) strain to constitutively produce ABAB, an anti-toxin against TcdA and TcdB of CDiff, intended to reduce the risk of CDI recurrence.
위약 비교기: Part A Cohort 2 Arm Placebo
Healthy adults administered 2 capsules of placebo orally QH12 for 28 days. N=2
The placebo is a capsule filled with commercially sourced pharmaceutical-grade microcrystalline cellulose (MCC), an inert substance. No anticipated risk related to the study product.
실험적: Part A Cohort 3 Arm FZ002
Healthy adults administered 1 capsule of FZ002 orally QH12 for 28 days. N=12
A recombinant live biotherapeutic product (rLBP) for oral administration, bioengineered from the parental S. boulardii (Sb) strain to constitutively produce ABAB, an anti-toxin against TcdA and TcdB of CDiff, intended to reduce the risk of CDI recurrence.
위약 비교기: Part A Cohort 3 Arm Placebo
Healthy adults administered 1 capsule of placebo orally QH12 for 28 days. N=2
The placebo is a capsule filled with commercially sourced pharmaceutical-grade microcrystalline cellulose (MCC), an inert substance. No anticipated risk related to the study product.
실험적: Part A Cohort 4 Arm FZ002
Healthy adults administered with 1 capsule of FZ002 orally once daily for 28 days. N=12
A recombinant live biotherapeutic product (rLBP) for oral administration, bioengineered from the parental S. boulardii (Sb) strain to constitutively produce ABAB, an anti-toxin against TcdA and TcdB of CDiff, intended to reduce the risk of CDI recurrence.
위약 비교기: Part A Cohort 4 Arm Placebo
Healthy adults administered with 1 capsule of placebo orally once daily for 28 days. N=2
The placebo is a capsule filled with commercially sourced pharmaceutical-grade microcrystalline cellulose (MCC), an inert substance. No anticipated risk related to the study product.
실험적: Part B Cohort 5 Arm FZ002
"some-risk" adults administered with 1 capsule of FZ002 orally once daily for 28 days. N=4
A recombinant live biotherapeutic product (rLBP) for oral administration, bioengineered from the parental S. boulardii (Sb) strain to constitutively produce ABAB, an anti-toxin against TcdA and TcdB of CDiff, intended to reduce the risk of CDI recurrence.
위약 비교기: Part B Cohort 5 Arm Placebo
"some-risk" adults administered with 1 capsule of placebo orally once daily for 28 days. N=1
The placebo is a capsule filled with commercially sourced pharmaceutical-grade microcrystalline cellulose (MCC), an inert substance. No anticipated risk related to the study product.
실험적: Part B Cohort 6 Group 1 Arm FZ002
"some-risk" adults administered with 4 capsules of FZ002 orally QH12 for 28 days. N=12
A recombinant live biotherapeutic product (rLBP) for oral administration, bioengineered from the parental S. boulardii (Sb) strain to constitutively produce ABAB, an anti-toxin against TcdA and TcdB of CDiff, intended to reduce the risk of CDI recurrence.
위약 비교기: Part B Cohort 6 Group 1 Arm Placebo
"some-risk" adults administered with 4 capsules of placebo orally QH12 for 28 days. N=3
The placebo is a capsule filled with commercially sourced pharmaceutical-grade microcrystalline cellulose (MCC), an inert substance. No anticipated risk related to the study product.
실험적: Part B Cohort 6 Group 2 Arm FZ002
"some-risk" adults administered with 1 capsule of FZ002 orally once daily for 28 days. N=8
A recombinant live biotherapeutic product (rLBP) for oral administration, bioengineered from the parental S. boulardii (Sb) strain to constitutively produce ABAB, an anti-toxin against TcdA and TcdB of CDiff, intended to reduce the risk of CDI recurrence.
위약 비교기: Part B Cohort 6 Group 2 Arm Placebo
"some-risk" adults administered with 1 capsule of placebo orally once daily for 28 days. N=2
The placebo is a capsule filled with commercially sourced pharmaceutical-grade microcrystalline cellulose (MCC), an inert substance. No anticipated risk related to the study product.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Occurrence of serious adverse events (SAEs)
기간: Through Day 208
Through Day 208
Occurrence of solicited adverse events (AEs)
기간: Through Day 35
Solicited AEs will include headache, fever, nausea, abdominal pain, diarrhea, malaise, constipation, fatigue, and vomiting. Oral temperatures will be measured daily.
Through Day 35
Occurrence of unsolicited AEs
기간: Through Day 57
Through Day 57
The occurrence of any positive yeast blood culture for Saccharomyces
기간: Days 8 and 29
Days 8 and 29

2차 결과 측정

결과 측정
측정값 설명
기간
The occurrence of abnormalities in clinical safety laboratory parameters based on change from baseline
기간: Days 8 and 29
laboratory parameters include White blood cell [WBC], Absolute neutrophil count [ANC], Hemoglobin [Hg], Platelets [PLT], creatinine, Alanine aminotransferase [ALT], Aspartate aminotransferase [AST], and total bilirubin
Days 8 and 29

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 6월 15일

기본 완료 (추정된)

2028년 8월 22일

연구 완료 (추정된)

2028년 9월 22일

연구 등록 날짜

최초 제출

2026년 6월 11일

QC 기준을 충족하는 최초 제출

2026년 6월 11일

처음 게시됨 (실제)

2026년 6월 16일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 6월 16일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 6월 11일

마지막으로 확인됨

2026년 6월 4일

추가 정보

이 연구와 관련된 용어

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

미국 FDA 규제 기기 제품 연구

아니

미국에서 제조되어 미국에서 수출되는 제품

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

클로스트리디움 디피실 감염에 대한 임상 시험

구독하다