Certain 3-azabicyclo[3.1.0]hexanes as GLP-1 receptor modulators

A compound of Formula (I)

• wherein
• X1 is N or C;
• X2 is independently N or C, provided that no more than two atoms in the aromatic ring A are N;
• Z1 is N or CR3;
• Z2 and Z3 are each independently N or CR4, provided that when Z1 or Z3 is N, Z2 is CR4;
• R1 is 0, 1, 2 or 3 substituents independently selected from F, Cl, Br, CN, OCH3, OCFH2, OCF2H, OCF3, CH3, CFH2, CF2H and CF3;
• R2 is selected from F, Cl and CN;
• R3 is selected from H, F, Cl, N(CH3)2, C1-2alkyl and OC1-2alkyl, wherein said C1-2alkyl is substituted by 0, 1, 2 or 3 F;
• R4 is independently selected from H, F, Cl, OH, CH3, CFH2, CF2H, CF3, OCH3, OCFH2, OCF2H and OCF3;
• R5 is selected from H, CH3, CFH2, CF2H and CF3;
• R6 is selected from (4- to 6-membered)heterocycloalkyl, (5- to 6-membered)heteroaryl, CN, C1-4alkyl, O(C1-4alkyl), S(C1-4alkyl), cyclopropyl, cyclobutyl, O(cyclopropyl) or S(cyclopropyl), wherein said (4- to 6-membered)heterocycloalkyl and (5- to 6-membered)heteroaryl is substituted by 0 or 1 substituent selected from C1-2alkyl and wherein said C1-4alkyl is substituted by 0 or 1 substituent selected from CN or OCH3, and 0, 1, 2 or 3 F and wherein said cyclopropyl and cyclobutyl is substituted by 0 or 1 substituent selected from CN, OCH3, OCFH2, OCF2H, OCF3 and CH2CN and 0, 1, 2 or 3 F;
• R7 is independently selected from F, C1-2alkyl and OC1-2alkyl, wherein said C1-2alkyl is substituted by 0, 1, 2 or 3 F;
• m is 1, 2 or 3;
• n is 0 or 1;
• p is 1, 2 or 3;
• and
• q is 0, 1 or 2;
• or a pharmaceutically acceptable salt thereof.