EXPANDED-ACCESS PROGRAM FOR THE TREATMENT OF CHRONIC HEPATITIS D WITH BRELOVITUG

Who cannot join

• Eligible and access to any ongoing CHD clinical trials designed to establish safety and efficacy.
• Pregnant, intends to become pregnant or lactating females.
• Known hypersensitivity to brelovitug or any of its excipients.
• Any clinically significant medical condition, comorbidity, laboratory abnormality, or other clinical circumstance that, in the judgment of the treating physician and/or Sponsor's Medical Reviewer, would place the patient at an unacceptable risk from treatment with brelovitug or result in an unfavorable benefit-risk assessment. Such conditions may include, but are not limited to, clinically significant cardiovascular, hepatic, gastrointestinal, pulmonary, neurologic, infectious, or renal disease.
• Current or prior hepatic decompensation (ascites, hepatic encephalopathy, variceal hemorrhage, etc) or Child-Turcotte-Pugh (CTP) Class B or C cirrhosis.
• Clinically significant liver disease attributable to an etiology other than HBV or HDV that, in the judgment of the treating physician and/or Sponsor's Medical Reviewer, would result in an unfavorable benefit-risk assessment for treatment with brelovitug. Patients with compensated cirrhosis up to CPT A6 may be considered on a case-by-case basis following review and approval by the Sponsor's Medical Reviewer, provided the potential benefits of treatment are considered to justify the potential risks.
• Presence of any disease, condition, concomitant therapy, or other clinical circumstance that is known or reasonably expected to significantly alter the absorption, distribution, metabolism, or excretion of brelovitug, or otherwise adversely affect its safety or intended pharmacologic activity, and that, in the judgment of the treating physician and/or Sponsor's Medical Reviewer, would make treatment with brelovitug clinically inappropriate.