Oligonucleotide-containing pharmacological compositions and their use
The present invention relates to methods and compositions containing oligonucleotides suitable for administration to humans and other mammals.
1. A composition suitable for administration in a mammal suffering from a pathological disorder or disease comprising two or more modified oligonucleotides, wherein
a.) a first and a second modified oligonucleotide each comprise about seven to seventy-five nucleotides containing seven or more contiguous ribose groups linked by achiral 5′ to 3′ internucleotide phosphate linkages, wherein said ribose groups of said modified oligonucleotides have a 2′ modification, and wherein said 5′ and 3′ ends of said modified oligonucleotides are blocked;
b.) said first modified oligonucleotide is complementary to a region of a first gene associated with said pathological disorder or disease and said second modified oligonucleotide is complementary to a region of a second gene associated with said pathological disorder or disease, wherein the sequence of each of said modified oligonucleotides is selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 6, SEQ ID NO: 10, SEQ ID NO: 12 and SEQ ID NO: 24; and
c.) wherein said first and second modified oligonucleotides are present in a total amount of less than about 7 mg.
2. The composition of claim 1 , wherein said composition comprises more than two modified oligonucleotides each comprising about seven to seventy-five nucleotides containing seven or more contiguous ribose groups linked by achiral 5′ to 3′ internucleotide phosphate linkages; wherein each of said more than two modified oligonucleotides is complementary to a region of a gene associated with said pathological disorder or disease, wherein the sequence of each of said modified oligonucleotides is selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 6, SEQ ID NO: 10, SEQ ID NO: 12 and SEQ ID NO: 24; and wherein said more than two modified oligonucleotides are present in a total amount of less than 7 mg.
3. A composition suitable for administration in a mammal suffering from a pathological disorder or disease comprising two or more modified oligonucleotides, wherein
a.) a first and a second modified oligonucleotide each comprise about seven to seventy-five nucleotides containing seven or more contiguous ribose groups linked by achiral 5′ to 3′ internucleotide phosphate linkages, wherein said ribose groups of said modified oligonucleotides have a 2′ modification, and wherein said 5′ and 3′ ends of said modified oligonucleotides are blocked;
b.) said first modified oligonucleotide is complementary to a region of a first gene associated with said pathological disorder or disease and said second modified oligonucleotide is complementary to a region of a second gene associated with said pathological disorder or disease, wherein said first modified oligonucleotide is modified CGTGTCAGGAGAAC (SEQ ID NO: 1); and said second modified oligonucleotide is modified TCTACAGTTCAGTCGA (SEQ ID NO: 6); and
c.) wherein said first and second modified oligonucleotides are present in a total amount of less than about 7 mg.
4. The composition of claim 3 , wherein said composition comprises more than two modified oligonucleotides each comprising about seven to seventy-five nucleotides containing seven or more contiguous ribose groups linked by achiral 5′ to 3′ internucleotide phosphate linkages; wherein each of said more than two modified oligonucleotides is complementary to a region of a gene associated with said pathological disorder or disease; wherein said more than two modified oligonucleotides are present in a total amount of less than 7 mg; and wherein a third modified oligonucleotide is modified GAACAGTTCGTCCATG (SEQ ID NO: 10).
5. The composition of claim 4 , wherein a fourth modified oligonucleotide is modified GGAGGGCATGGCGCGG (SEQ ID NO: 12).
6. The composition of claim 5 , wherein a fifth modified oligonucleotide is modified CATGGTCACGTCCTGC (SEQ ID NO: 24).