A Study of SAR444245 With or Without Other Anticancer Therapies for the Treatment of Adults and Adolescents With Relapsed or Refractory B Cell Lymphoma (Master Protocol) [Pegathor Lymphoma 205]

The duration of the study for an individual participant started from the signature of the main informed consent and included: a screening period of up to 28 days; a treatment period \[max\] 35 cycles (21 days per cycle) for Cohort A and 52 cycles (14 days per cycle) for Cohort C1 or until occurrence of unacceptable toxicities or until PD; an end-of-treatment visit at least approximately 30 days following the last administration of study drug (or until the participant receives another anticancer therapy, whichever is earlier); and a follow-up visits 3 months after treatment discontinuation and every 3 months thereafter following, until disease progression, or initiation of another antitumor treatment, or death, whichever is earlier.

Age

12–any

Sex

ALL

Healthy volunteers

Not accepted

You may be eligible if

Participants must have been ≥ 12 years of age, at the time of signing the informed consent
Disease location was amenable to tumor biopsy at baseline
All participants must have had a measurable disease
Both male and female participants agreed to use approved contraception methods; not pregnant or breastfeeding for female participants; no donation or cryopreservation of eggs (ova, oocytes) for female participants and sperms for male participants.
Had to be capable of giving signed informed consent
For cohort A: Histologically or cytologically confirmed diagnosis of classic Hodgkin lymphoma (cHL), must have received at least two prior lines of systemic therapy for cHL, including at least one containing an anthracycline or brentuximab.
For cohort C1: Histologically confirmed diagnosis of diffuse large B Cell lymphoma (DLBCL), must have received at least two prior lines of systemic therapy for DLBCL, including one containing a combination of anthracycline and rituximab (or another anti-CD20 agent), with the last line of therapy a Health Authority approved CD19-directed CAR-T therapy. Patients must have BOR (Best Overall Response) of stable disease (SD) or progressive disease (PD) after CD-19 directed CAR-T therapy.

You may not be if

Participants were excluded from the study if any of the following criteria applied:
Eastern Cooperative Oncology Group (ECOG) performance status of ≥ 2 (≥ 16 years old). Lansky Scale (\< 16 years old) ≤ 60%
Poor bone marrow reserve
Poor organ function
Participants with baseline oxygen saturation (SpO2) ≤ 92% (without oxygen therapy)
Lymphomatous involvement of the central nervous system
History of allogenic or solid organ transplant
Prior IV or subcutaneous anticancer therapy, investigational agent, major surgery within 21 days prior to initiation of IMP; oral anticancer therapy within 5 half-lives or completed palliative radiotherapy within 21 days prior to initiation of IMP
Has received prior IL-2-based anticancer treatment
Comorbidity requiring corticosteroid therapy
Antibiotic use (excluding topical antibiotics) ≤ 14 days prior to first dose of IMP
Severe or unstable cardiac condition within 6 months prior to starting study treatment
Had active, known, or suspected autoimmune disease that has required systemic treatment in the past 2 years-Known second malignancy either progressing or requiring active treatment within the last 3 years
Receipt of a live or live attenuated virus vaccination within 28 days of planned treatment start. Seasonal flu vaccines or SARS-CoV-2 vaccine that do not contain live virus were permitted
The above information is not intended to contain all considerations relevant to the potential participation in a clinical trial.

What this study is about