Abstract: A foldable litter box and a litter box with a variable volume are provided. The foldable litter box includes a bottom plate and a several side plates integrally formed with the bottom plate, the side plates can be bended relative to the bottom plate to enclose a housing cavity. The side plates includes a front baffle and a rear baffle, as well as a left baffle and right baffle. The foldable litter box also includes connection plates integrally formed with the front baffle and the rear baffle, and the connection plates can be bent and connected to the left baffle and the right baffle respectively. The litter box can be quickly transformed into a pet litterbox with different volume from a flat state to different folded states, and the litter box can be quickly returned to the flat state when not in use, thus reducing space occupation.

Abstract: A pet litter scoop assembly and a litter sieve are related, the pet litter scoop assembly including the litter sieve for collecting used litter. The litter sieve includes a base part and a handle extending from the base part, the base part including a bottom wall and a sidewall extending upwardly from the bottom wall, with a sieving cavity formed by the sidewall and the bottom wall, the handle connected to the sidewall. The litter sieve includes holes penetrating the bottom wall and sized such that the used litter cannot pass through the holes, and at least one guiding rib(s) protruding from the bottom wall to the sieving cavity and positioned adjacent to the holes to guide unused litter pellets in the sieving cavity to pass through the holes. The litter sieve and litter scoop assembly can help to avoid blocking of the holes.

Abstract: A foldable litter box and a litter box with a variable volume are provided. The foldable litter box includes a bottom plate and a several side plates integrally formed with the bottom plate, the side plates can be bended relative to the bottom plate to enclose a housing cavity. The side plates includes a front baffle and a rear baffle, as well as a left baffle and right baffle. The foldable litter box also includes connection plates integrally formed with the front baffle and the rear baffle, and the connection plates can be bent and connected to the left baffle and the right baffle respectively. The litter box can be quickly transformed into a pet litterbox with different volume from a flat state to different folded states, and the litter box can be quickly returned to the flat state when not in use, thus reducing space occupation.

Abstract: A pet litter scoop assembly and a litter sieve are related, the pet litter scoop assembly including the litter sieve for collecting used litter. The litter sieve includes a base part and a handle extending from the base part, the base part including a bottom wall and a sidewall extending upwardly from the bottom wall, with a sieving cavity formed by the sidewall and the bottom wall, the handle connected to the sidewall. The litter sieve includes holes penetrating the bottom wall and sized such that the used litter cannot pass through the holes, and at least one guiding rib(s) protruding from the bottom wall to the sieving cavity and positioned adjacent to the holes to guide unused litter pellets in the sieving cavity to pass through the holes. The litter sieve and litter scoop assembly can help to avoid blocking of the holes.

Abstract: The present disclosure relates to methods of treating cancers comprising coadministration of mirdametinib or a pharmaceutically acceptable salt form thereof, and lifirafenib or a pharmaceutically acceptable salt form thereof, to a patient in need thereof. Also disclosed are pharmaceutical compositions of mirdametinib or a pharmaceutically acceptable salt form thereof, and lifirafenib or a pharmaceutically acceptable salt form thereof, for use in such cancer treatment, as well as uses of these compounds for manufacture of medicaments for the treatment of cancers.

Abstract: Disclosed herein is a pharmaceutical combination for use in the prevention, delay of progression or treatment of cancer, wherein the pharmaceutical combination exhibits a synergistic efficacy. The pharmaceutical combination comprises a humanized antagonist monoclonal antibody against PD- and a RAF inhibitor. Also disclosed herein is a combination for use in the prevention, delay of progression or treatment of cancer in a subject, comprising administering to the subject a therapeutically effective amount of a humanized antagonist monoclonal antibody against PD-1 and a therapeutically effective amount of a RAF inhibitor.

Abstract: An information transmission method is provided, including: A control device obtains a second universal serial bus video class UVC port and a second virtual network port based on configuration of a universal serial bus USB port of the control device. The control device determines address information of a camera device, where a first UVC port and a first virtual network port are configured on the camera device, and the first UVC port and the first virtual network port are obtained based on configuration of a USB port of the camera device. The control device sends the address information to the camera device through a UVC channel, where the UVC channel is established based on the first UVC port and the second UVC port.

Abstract: Disclosed herein is a method for the prevention, delay of progression or treatment of cancer in a subject, comprising administering to the subject in need thereof a PARP inhibitor, particularly, (R)-2-fluoro-10a-methyl-7,8,9,10,10a,11-hexahydro-5,6,7a,11-tetraazacyclohepta[def]cyclopenta[a]fluoren-4(5H)-one, a sesqui-hydrate thereof, or a pharmaceutically acceptable salt thereof, in combination with an immune checkpoint inhibitor or a chemotherapeutic agent. Also, disclosed a pharmaceutical combination comprising a PARP inhibitor, particularly, (R)-2-fluoro-10a-methyl-7,8,9,10,10a,11-hexahydro-5,6,7a,11-tetraazacyclohepta[def]cyclopenta[a]fluoren-4(5H)-one, a sesqui-hydrate thereof, or a pharmaceutically acceptable salt thereof, in combination with an immune checkpoint inhibitor, or a chemotherapeutic agent and the use thereof.

Abstract: Disclosed herein is a pharmaceutical combination for use in the prevention, delay of progression or treatment of cancer, wherein the pharmaceutical combination exhibits a synergistic efficacy. The pharmaceutical combination comprises a humanized antagonist monoclonal antibody against PD- and a RAF inhibitor. Also disclosed herein is a combination for use in the prevention, delay of progression or treatment of cancer in a subject, comprising administering to the subject a therapeutically effective amount of a humanized antagonist monoclonal antibody against PD-1 and a therapeutically effective amount of a RAF inhibitor.

Abstract: Disclosed herein is a pharmaceutical combination for use in the prevention, delay of progression or treatment of cancer, wherein the pharmaceutical combination exhibits a synergistic efficacy. The pharmaceutical combination comprises a humanized antagonist monoclonal antibody against PD- and a RAF inhibitor. Also disclosed herein is a combination for use in the prevention, delay of progression or treatment of cancer in a subject, comprising administering to the subject a therapeutically effective amount of a humanized antagonist monoclonal antibody against PD-1 and a therapeutically effective amount of a RAF inhibitor.

Abstract: Disclosed herein is a method for the prevention, delay of progression or treatment of cancer in a subject, comprising administering to the subject in need thereof a PARP inhibitor, particularly, (R)-2-fluoro-10a-methyl-7, 8, 9, 10, 10a, 11-hexahydro-5, 6, 7a, 11-tetraazacyclohepta [def] cyclopenta [a] fluoren-4 (5H)-one, a sesqui-hydrate thereof, or a pharmaceutically acceptable salt thereof, in combination with temozolomide and/or radiation therapy. Also, disclosed a pharmaceutical combination comprising a PARP inhibitor, particularly, (R)-2-fluoro-10a-methyl-7, 8, 9, 10, 10a, 11-hexahydro-5, 6, 7a, 11-tetraazacyclohepta [def] cyclopenta [a] fluoren-4 (5H)-one, a sesqui-hydrate thereof, or a pharmaceutically acceptable salt thereof, in combination with temozolomide and the use thereof.

Abstract: Disclosed herein is a pharmaceutical combination for use in the prevention, delay of progression or treatment of cancer, wherein the pharmaceutical combination exhibits a synergistic efficacy. The pharmaceutical combination comprises a humanized antagonist monoclonal antibody against PD- and a RAF inhibitor. Also disclosed herein is a combination for use in the prevention, delay of progression or treatment of cancer in a subject, comprising administering to the subject a therapeutically effective amount of a humanized antagonist monoclonal antibody against PD-1 and a therapeutically effective amount of a RAF inhibitor.

Abstract: Disclosed herein is a method for the prevention, delay of progression or treatment of cancer in a subject, comprising administering to the subject in need thereof a PARP inhibitor, particularly, (R)-2-fluoro-10a-methyl-7,8,9,10,10a,11-hexahydro-5,6,7a,11-tetraazacyclohepta[def]cyclopenta[a]fluoren-4(5H)-one, a sesqui-hydrate thereof, or a pharmaceutically acceptable salt thereof, in combination with an immune checkpoint inhibitor or a chemotherapeutic agent. Also, disclosed a pharmaceutical combination comprising a PARP inhibitor, particularly, (R)-2-fluoro-10a-methyl-7,8,9,10,10a,11-hexahydro-5,6,7a,11-tetraazacyclohepta[def]cyclopenta[a]fluoren-4(5H)-one, a sesqui-hydrate thereof, or a pharmaceutically acceptable salt thereof, in combination with an immune checkpoint inhibitor, or a chemotherapeutic agent and the use thereof.

Abstract: A method for establishing a neighbor relationship, where corresponding authentication information is added to packets that are sent from a first network device and a second network device to each other. The first network device sends a hello packet to the second network device. The second network device receives the hello packet, performs authentication, and responds to the hello packet using an extended unidirectional link (UDL) link state packet (LSP) when the authentication succeeds. The first network device receives the extended UDL LSP, and performs authentication. When an authentication result includes that both the first network device and the second network device enable authentication and the authentication succeeds, a neighbor relationship between the first network device and the second network device may be established.

Abstract: A method for establishing a neighbor relationship, where corresponding authentication information is added to packets that are sent from a first network device and a second network device to each other. The first network device sends a hello packet to the second network device. The second network device receives the hello packet, performs authentication, and responds to the hello packet using an extended unidirectional link (UDL) link state packet (LSP) when the authentication succeeds. The first network device receives the extended UDL LSP, and performs authentication. When an authentication result includes that both the first network device and the second network device enable authentication and the authentication succeeds, a neighbor relationship between the first network device and the second network device may be established.