DARTAcceptedBeyond the letter
No developmental and reproductive toxicology studies
Why: Patient population nearly exclusively male; no adverse findings in toxicology studies · Other reason · Weight of evidence
“Per the applicant, developmental and reproductive toxicology studies have not been conducted with SRP-9001 for the following reasons:”
✓ VerifiedFDA pharmacology/toxicology review, p. 47Source ↗ “Animal reproductive and developmental toxicity and carcinogenicity studies were not conducted with ELEVIDYS, which is acceptable based on the patient population and lack of ELEVIDYS-related adverse findings in the toxicology studies.”
✓ VerifiedFDA pharmacology/toxicology review, p. 3Source ↗ CarcinogenicityAcceptedBeyond the letter
No carcinogenicity/tumorigenicity studies
Why: No cancer reported across 162 AAV clinical trials; no concerning findings in completed toxicology studies · Human data · Class precedent · Weight of evidence
“Per the applicant, carcinogenicity/tumorigenicity studies have not been conducted with SRP-9001 for the following reasons: • AAV of various serotypes including AAV2 and AAVrh74, have been studied in 162 clinical trials; thus far, no cancer of any type has been reported.”
✓ VerifiedFDA pharmacology/toxicology review, p. 48Source ↗ “Reviewer Comment: Based on the indication of X-linked DMD which occurs primarily in males and lack of concerning findings in the completed toxicology studies, further assessment of developmental and reproductive toxicology, carcinogenicity/tumorigenicity, and genotoxicity are not warranted at this time.”
✓ VerifiedFDA pharmacology/toxicology review, p. 48Source ↗ GenotoxicityAcceptedBeyond the letter
No genotoxicity studies; integration risk addressed by literature
Why: Literature supports random AAV integration at low frequencies · Class precedent · Low-risk modality
“Per the applicant, genotoxicity studies have not been conducted with SRP-9001 because the literature thus far, supports random integration of AAV vector into the host genome at low frequencies”
✓ VerifiedFDA pharmacology/toxicology review, p. 48Source ↗ “Reviewer Comment: Based on the indication of X-linked DMD which occurs primarily in males and lack of concerning findings in the completed toxicology studies, further assessment of developmental and reproductive toxicology, carcinogenicity/tumorigenicity, and genotoxicity are not warranted at this time.”
✓ VerifiedFDA pharmacology/toxicology review, p. 48Source ↗ Safety pharmacologyVerdict not stated
No safety pharmacology studies
“There were no safety pharmacology studies performed with SRP-9001.”
✓ VerifiedFDA pharmacology/toxicology review, p. 31Source ↗