A Phase 1/2 Study of Oncobax®-AK Administered in Combination With Immunotherapy To Patients With Advanced Solid Tumors

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Akkermansia muciniphila is a naturally occurring bacterium found in the healthy human gastrointestinal tract. Analysis of the gut microbiota of NSCLC or RCC patients shows that the presence of Akkermansia is associated with the clinical efficacy of immunotherapy. In preclinical models, oral administration of the Akkermansia p2261 strain reverses resistance to PD-1 blockade. In the clinical setting, it is therefore hypothesized that the oral administration of Oncobax®-AK to cancer patients under immunotherapy, but whose gut microbiota is deficient in Akkermansia will restore / improve the efficacy of immunotherapy in patients with NSCLC or RCC.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age \> 18 years

• Histologically confirmed Stage IV non-squamous NSCLC or clear cell RCC

• NSCLC-specific criterion: Best tumor response (by iRECIST) as Stable Disease

• NSCLC-specific criterion: PD-L1 expression \> 50%

• ECOG Performance Status = 0-1

• Negative stool PCR test for Akkermansia

• At least one measurable lesion per iRECIST

• Hemoglobin ≥ 100 g/L

• Albumin \> 35 g/L

⁃ Signed informed consent

Locations
Other Locations
Belgium
CHU Ambroise Paré
RECRUITING
Mons
France
Centre Georges Francois Leclerc
RECRUITING
Dijon
Institut Gustave Roussy
RECRUITING
Paris
ICANS - Institut de cancérologie Strasbourg
RECRUITING
Strasbourg
Contact Information
Primary
Alain Thibault, MD
alain.thibault@everimmune.com
+32472196345
Time Frame
Start Date: 2022-10-01
Estimated Completion Date: 2026-06
Participants
Target number of participants: 122
Treatments
Experimental: Phase 2 - NSCLC
Oncobax-AK (1 capsule) will be administered daily until PD\< excessive toxicity or withdrawal of consent
Experimental: Phase 2 -RCC
Oncobax-AK (1 capsule) will be administered daily until PD\< excessive toxicity or withdrawal of consent
Sponsors
Leads: EverImmune

This content was sourced from clinicaltrials.gov