Antisense oligomers and methods of using the same for treating diseases associated with the acid alpha-glucosidase gene
The present disclosure relates to modified antisense oligonucleotides. The nucleotides described herein are of 10 to 40 nucleobases and include a targeting sequence complementary to a target region within intron 1 of a pre-mRNA of the human alpha glucosidase (GAA) gene. The target region includes at least one additional nucleobase compared to the targeting sequence, wherein the at least one additional nucleobase has no complementary nucleobase in the targeting sequence, and wherein the at least one additional nucleobase is internal to the target region.
1. A modified antisense oligonucleotide of 10 to 40 nucleobases, or a pharmaceutically acceptable salt thereof, comprising a targeting sequence complementary to a target region within intron 1 of a pre-mRNA of the human alpha glucosidase (GAA) gene (SEQ ID NO: 1), wherein the target region comprises at least one additional nucleobase compared to the targeting sequence, and wherein the at least one additional nucleobase is internal to the target region.
2. The modified antisense oligonucleotide, or a pharmaceutically acceptable salt thereof, of claim 1 , wherein the target region comprises at least one of SEQ ID NO: 2 or SEQ ID NO: 3.
3. The modified antisense oligonucleotide of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the antisense oligonucleotide promotes retention of exon 2 in the GAA mRNA upon binding of the targeting sequence to the target region.
4. The modified antisense oligonucleotide of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the target region comprises from one to three additional nucleobases compared to the targeting sequence.
5. The modified antisense oligonucleotide of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the antisense oligonucleotide induces GAA enzyme activity at least-two-fold according to an enzyme activity test as compared to a second antisense oligonucleotide that is fully complementary to the target region within SEQ ID NO: 1.
6. The modified antisense oligonucleotide of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the targeting sequence is selected from any one of SEQ ID NOs: 33-42.
7. A pharmaceutical composition comprising: (a) a pharmaceutically acceptable carrier and (b) a modified antisense oligonucleotide of 10 to 40 nucleobases, or a pharmaceutically acceptable salt thereof, comprising a targeting sequence complementary to a target region within intron 1 of a pre-mRNA of the human alpha glucosidase (GAA) gene (SEQ ID NO: 1), wherein the target region comprises at least one additional nucleobase compared to the targeting sequence, and wherein the at least one additional nucleobase is internal to the target region.
8. The modified antisense oligonucleotide of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the targeting sequence is SEQ ID NO: 33.
9. The modified antisense oligonucleotide of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the targeting sequence is SEQ ID NO: 34.
10. The modified antisense oligonucleotide of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the targeting sequence is SEQ ID NO: 35.
11. The modified antisense oligonucleotide of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the targeting sequence is SEQ ID NO: 36.
12. The modified antisense oligonucleotide of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the targeting sequence is SEQ ID NO: 37.
13. The modified antisense oligonucleotide of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the targeting sequence is SEQ ID NO: 38.
14. The modified antisense oligonucleotide of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the targeting sequence is SEQ ID NO: 45.
15. The modified antisense oligonucleotide of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the targeting sequence is SEQ ID NO: 46.
16. The modified antisense oligonucleotide of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the at least one additional nucleobase is cytosine.