CELL-REACTIVE, LONG-ACTING, OR TARGETED COMPSTATIN ANALOGS AND USES THEREOF
In some aspects, the present invention provides cell-reactive compstatin analogs and compositions comprising cell-reactive compstatin analogs. In some aspects, the invention further provides methods of using cell-reactive compstatin analogs, e.g., to inhibit complement-mediated damage to a cell, tissue, or organ. In some aspects, the invention provides long-acting compstatin analogs and compositions comprising long-acting compstatin analogs. In some aspects, the invention further provides methods of using long-acting compstatin analogs, e.g., to inhibit complement-mediated damage to a cell, tissue, or organ. In some aspects, the invention provides targeted compstatin analogs and compositions comprising targeted compstatin analogs. In some aspects, the invention further provides methods of using targeted compstatin analogs, e.g., to inhibit complement-mediated damage to a cell, tissue, or organ.
1 . A physiologically acceptable or pharmaceutical grade composition comprising a cell-reactive compstatin analog.
2 .- 136 . (canceled)
137 . A method of treating a subject in need of treatment for a complement-mediated disorder, the method comprising administering a long-acting compstatin analog to the subject, wherein the long-acting compstatin analog comprises one or more clearance reducing moieties attached to one or more compstatin analog moieties, wherein:
each compstatin analog moiety comprises a cyclic peptide having an amino acid sequence as set forth in any of SEQ ID NOs: 3-36, extended by one or more terminal amino acids at the N-terminus, C-terminus, or both, wherein the one or more amino acids has a side chain comprising a primary or secondary amine and is separated from the cyclic peptide by a rigid or flexible spacer comprising an oligo(ethylene glycol) moiety that is (—(O—CH 2 CH 2 —) n ), wherein n is between 1 and 500,
so that the compstatin analog moiety comprises the cyclic peptide, linked via its N-terminus or C-terminus to the spacer, which is linked to the one or more amino acids; and
each clearance-reducing moiety comprises a polyethylene glycol (PEG) and is covalently attached via a linking moiety to the side chain comprising a primary or a secondary amine, wherein the linking moiety comprises an unsaturated alkyl moiety, a moiety comprising a nonaromatic cyclic ring system, an aromatic moiety, an ether moiety, an amide moiety, an ester moiety, a carbonyl moiety, an imine moiety, a thioether moiety, or an amino acid residue,
wherein the clearance-reducing moiety and the spacer are separated by the one or more amino acids comprising a side chain having a primary or secondary amine,
so that the compstatin analog comprises the cyclic peptide linked via its N-terminus or C-terminus to the spacer, which is linked to the one or more amino acids, which in turn is linked to the linking moiety and the clearance-reducing moiety.
138 . A method of making the long-acting compstatin analog of claim 137 , comprising reacting the compound of any of Formulae I-XVI or Formulae A-H with a compstatin analog moiety comprising a cyclic peptide, wherein the amino acid sequence of the cyclic peptide is SEQ ID NO: 3-36:
wherein the reactive functional group is selected from the group consisting of sulfates, imidates, ortho esters, sulfites, carbamates and N-hydroxysuccinimide esters.
139 . A long-acting compstatin analog comprising one or more clearance reducing moieties attached to one or more compstatin analog moieties, wherein:
(a) each compstatin analog moiety comprises a cyclic peptide extended by one or more amino acids at the N-terminus, C-terminus, or both, wherein the cyclic peptide comprises the amino acid sequence of SEQ ID NO: 8 having 2, 3, or 4 substitutions,
wherein the cyclic peptide:
(i) has a tryptophan analog selected from the group consisting of 2-naphthylalanine (2-NaI), 1-naphthylalanine (1-NaI), 2-indanylglycine carboxylic acid (Ig1), dihydrotrpytophan (Dht), 4-benzoyl-L-phenylalanine, β-3-benzothienyl-L-alanine, 1-methyltryptophan, and 5-methyltryptophan at position 4 relative to SEQ ID NO:8;
(ii) has a tryptophan or 5-fluorotryptophan at position 7 relative to SEQ ID NO:8; and
(ii) has an alanine or 2-aminobutyric acid (2-Abu) at position 9 relative to SEQ ID NO:8; and
wherein the one or more amino acids has a side chain comprising a primary or secondary amine and is separated from the cyclic portion of the peptide by a rigid or flexible spacer comprising an oligo(ethylene glycol) moiety; and
(b) each clearance reducing moiety comprises a PEG.
140 . A method of protecting a cell from complement-mediated damage comprising contacting the cell with a long-acting compstatin analog, wherein the long-acting compstatin analog comprises one or more clearance reducing moieties attached to one or more compstatin analog moieties, wherein:
each compstatin analog moiety comprises a cyclic peptide having an amino acid sequence as set forth in any of SEQ ID NOs: 3-36, extended by one or more terminal amino acids at the N-terminus, C-terminus, or both, wherein the one or more amino acids has a side chain comprising a primary or secondary amine and is separated from the cyclic peptide by a rigid or flexible spacer comprising an oligo(ethylene glycol) moiety that is (—(O—CH 2 CH 2 —) n ), wherein n is between 1 and 500,
so that the compstatin analog moiety comprises the cyclic peptide, linked via its N-terminus or C-terminus to the spacer, which is linked to the one or more amino acids; and
each clearance-reducing moiety comprises a polyethylene glycol (PEG) and is covalently attached via a linking moiety to the side chain comprising a primary or a secondary amine, wherein the linking moiety comprises an unsaturated alkyl moiety, a moiety comprising a nonaromatic cyclic ring system, an aromatic moiety, an ether moiety, an amide moiety, an ester moiety, a carbonyl moiety, an imine moiety, a thioether moiety, or an amino acid residue,
wherein the clearance-reducing moiety and the spacer are separated by the one or more amino acids comprising a side chain having a primary or secondary amine,
so that the compstatin analog comprises the cyclic peptide linked via its N-terminus or C-terminus to the spacer, which is linked to the one or more amino acids, which in turn is linked to the linking moiety and the clearance-reducing moiety.
141 . The method of claim 140 , wherein the cell is in a subject and the method comprises administering one or more doses of the long-acting compstatin analog to the subject.
142 . The method of claim 140 , wherein the cell is a retinal cell.
143 . A method of protecting a cell from complement-mediated damage comprising contacting the cell with a long-acting compstatin analog, wherein the long-acting compstatin analog comprises one or more clearance reducing moieties attached to one or more compstatin analog moieties, wherein:
(a) each compstatin analog moiety comprises a cyclic peptide extended by one or more amino acids at the N-terminus, C-terminus, or both, wherein the cyclic peptide comprises the amino acid sequence of SEQ ID NO: 8 having 2, 3, or 4 substitutions,
wherein the cyclic peptide:
(i) has a tryptophan analog selected from the group consisting of 2-naphthylalanine (2-NaI), 1-naphthylalanine (1-NaI), 2-indanylglycine carboxylic acid (Ig1), dihydrotrpytophan (Dht), 4-benzoyl-L-phenylalanine, β-3-benzothienyl-L-alanine, 1-methyltryptophan, and 5-methyltryptophan at position 4 relative to SEQ ID NO:8;
(ii) has a tryptophan or 5-fluorotryptophan at position 7 relative to SEQ ID NO:8; and
(ii) has an alanine or 2-aminobutyric acid (2-Abu) at position 9 relative to SEQ ID NO:8; and
wherein the one or more amino acids has a side chain comprising a primary or secondary amine and is separated from the cyclic portion of the peptide by a rigid or flexible spacer comprising an oligo(ethylene glycol) moiety; and
(b) each clearance reducing moiety comprises a PEG.
144 . The method of claim 143 , wherein the one or more amino acids comprise a Lys residue.
145 . The method of claim 143 , wherein the oligo(ethylene glycol) moiety is (—(O—CH 2 —CH 2 —) n , wherein n is between 1 and 10.
146 . The method of claim 143 , wherein the spacer comprises —(CH 2 ) m — and —(O—CH 2 —CH 2 —) n joined covalently, wherein m is between 1 and 10 and n is between 1 and 10.
147 . The method of claim 143 , wherein the spacer comprises 8-amino-3,6-dioxaoctanoic acid (AEEAc) or 11-amino-3,6,9-trioxaundecanoic acid.
148 . The method of claim 143 , wherein the long-acting compstatin analog comprises a clearance-reducing moiety having a molecular weight of at least about 10 kD.
149 . The method of claim 143 , wherein the one or more clearance reducing moieties are attached directly or via a linking moiety to the one or more compstatin analog moieties.
150 . The method of claim 143 , wherein the one or more clearance reducing moieties are attached via a linking moiety to the one or more compstatin analog moieties, and wherein the linking moiety comprises an unsaturated alkyl moiety, a moiety comprising a nonaromatic cyclic ring system, an aromatic moiety, an ether moiety, an amide moiety, an ester moiety, a carbonyl moiety, an imine moiety, a thioether moiety, and/or an amino acid residue.
151 . The method of claim 143 , wherein the long-acting compstatin analog comprises a clearance-reducing moiety having a molecular weight of between about 20 kD and about 100 kD.
152 . The method of claim 143 , wherein the long-acting compstatin analog comprises a clearance-reducing moiety having a molecular weight of at least about 40 kilodaltons (kD).
153 . The method of claim 143 , wherein the clearance reducing moiety comprises a linear PEG.
154 . The method of claim 143 , wherein the clearance reducing moiety comprises a linear PEG and the compstatin analog moiety is attached at each end of the linear PEG.
155 . The method of claim 143 , wherein the long-acting compstatin analog comprises between 2 and 10 compstatin analog moieties.
156 . The method of claim 143 , wherein the long-acting compstatin analog has a plasma half-life of at least 4 days when injected intravenously into a primate.
157 . The method of claim 143 , wherein the cell is in a subject and the method comprises administering one or more doses of the long-acting compstatin analog to the subject.
158 . The method of claim 143 , wherein the cell is a retinal cell.