Long-term Safety and Efficacy Evaluation of Lunsekimig (SAR443765) in Adult Participants With Asthma

Prior treatment

• Participant who developed a new medical condition or a change in status of an established medical condition or requires a new treatment or medication prior to enrollment that, per Investigator's medical judgement would adversely affect participation of the participant in this study or would require permanent lunsekimig discontinuation, or participants potentially at risk of noncompliance to study procedures
• Prescription drug or substance abuse, including alcohol, considered significant by the Investigator
• Participants who are receiving prohibited concomitant medications
• Participants who, during their participation in the parent study, developed an AE or an SAE deemed related to lunsekimig, which in the opinion of the Investigator could indicate that continued treatment with lunsekimig may present an unreasonable risk for the participant
  • The above information is not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.

Other illness

• Participant who was diagnosed with a new pulmonary disease which may impair lung function
• History of hypersensitivity or allergy to lunsekimig or to any of the excipients used in the presentation or in preparation for administration of lunsekimig, or other allergy that, in the opinion of the Investigator, contraindicates participation in the study

Other

• Participants are excluded from the study if any of the following criteria apply:
• Current smoker or active vaping of any products and/or marijuana smoking

• Participants who completed the treatment period of Study DRI16762 or ACT18301, including the EOT visit, as per protocol
• Participants with stable background therapy with moderate or high-dose ICS in combination with the following controller medications, as maintained during the respective parent study in which they have participated:
  • For Study DRI16762: At least 1 and no more than 2 additional controllers (eg, LABA, LAMA, LTRA, or methylxanthines), with or without oral prednisone
  • For Study ACT18301: LABA with or without LTRA
• Participants who are able and willing to participate in the open-label extension study, and to comply with requested study visits and procedures
• Contraception for male and female participants during the study intervention period and during 8 weeks following the last administration of study intervention. And:
  • For female participants:
• incapable of becoming pregnant, or
• not pregnant or breast feeding
• no eggs donation or cryopreserving eggs
  • For male participants:
  • \-- No sperm donation or cryopreserving sperm
  • \- Capable of giving signed informed consent