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Dado oficial do USPTO

ILLIMIS

Sabia que essa marca já está registrada no Estados Unidos?

Antes de investir em nome, identidade e divulgação, valide risco de colisão e estratégia de registro para não perder tempo nem budget.

Active USPTO registrationTipo: MistaEscritório: US

Snapshot rápido

ILLIMIS

ST13

US500000079342263

Classe

5, 42

Pedido

79342263

Registro

7095522

Diagnóstico de risco e oportunidade

Leitura executiva para decisão de naming, protocolo e monitoramento.

Atenção: há risco ativo

Situação USPTO

Active USPTO registration

Tipo de processo

Pedido e registro

Eventos registrados

27

Atualização mais recente

31/10/2023

Classificação

Registrada

Tipo de marca

Mista

Classes Nice

5, 42

Data de depósito

17/03/2022

Data de registro

04/07/2023

Data de expiração

-

Ação recomendada

Execute uma análise de colidência completa e valide classes antes de qualquer protocolo ou investimento de marca.

Próximo passo

Esses são os detalhes do processo de registro. Mesmo assim, o monitoramento constante é o que garante tranquilidade de que o seu principal ativo continue protegido.

Dados completos do processo

Campos estruturados da autoridade responsável e do histórico oficial.

Data da situação

04/07/2023

Última transação

04/07/2023

Escritório responsável

United States Patent and Trademark Office

Código da situação

700

Cadastro oficial

Principal Register

Código do desenho

5

Tipo de titular

03

Localização do titular

KR

Examinador

THOMAS, JULIE

Unidade examinadora

L70

Localização atual

PUBLICATION AND ISSUE SECTION

Titulares e representantes

Titulares

Illimis Therapeutics, Inc.

Representantes

Jong Park The PL Law Group, PLLC

Classificação técnica

Classes Nice

Classe 5Classe 42

Códigos Vienna

Sem códigos Vienna disponíveis.

Produtos e serviços

Classe 5

Pharmaceutical preparations for the treatment of auto-immune diseases; pharmaceutical agents affecting sensory organs; pharmaceutical agents affecting peripheral nervous system; pharmaceutical preparations for activating cellular function; pharmaceutical preparations acting on the central nervous system; pharmaceutical preparations for respiratory organs; pharmaceutical preparations for the prevention of disorders of the nervous system; pharmaceutical preparations for the treatment of cardiovascular disease; pharmaceutical preparations for the treatment of inflammatory diseases; ophthalmic preparations; pharmaceutical preparations for the treatment of eye diseases and conditions; pharmaceutical preparations for the treatment of degenerative brain disease; pharmaceutical preparations for the treatment of brain dysfunction; pharmaceutical preparations for the treatment of stroke; pharmaceutical preparations for the treatment of cerebrovascular disease; pharmaceutical preparations for the treatment of dementia; pharmaceutical preparations for the treatment of Alzheimer's disease; pharmaceutical preparations for use in the treatment of solid tumors and growthshemolytic diseases and disordersamyloidosismetabolic diseases and disorderslupusinflammation and autoimmune diseases and disorders

Classe 42

Pharmaceutical product development; pharmaceutical research and development of medicines in the field of age-related diseases/disorders and degenerative diseases; pharmaceutical research and development of medicines in the field of chronic malady/disease and dysfunction; scientific research for medical purposes in the field of gene therapy; medical scientific research in the field of brain disease; medical scientific research in the field of neurological diseases; biotechnology research and scientific and pharmaceutical research in the antibody field; biological research; scientific research in the field of cancer disease; remote monitoring and quality control inspection for others of active substances in the pharmaceutical research field and scientific analysis of active substances in the pharmaceutical research field; research for quality inspection related to human hygiene management for medical research purposes; scientific and medical research of autoimmune disease; development of pharmaceutical preparations for cell therapy; stem cell collection for medical research; cell processing and culture for medical research; pharmaceutical research and development of medicines in the field of inflammatory disease; pharmaceutical research and development of medicines in the field of eye disease; pharmaceutical research and development of medicines in the field of amyloidosis; consultancy pertaining to pharmacology relating to pharmaceutical quality control; providing information on the research of medical products relating to pharmaceutical quality control

Publicações

Histórico de despachos e eventos da marca no USPTO.

27 publicações encontradas

FINO

FINAL DECISION TRANSACTION PROCESSED BY IB

31/10/2023

FICS

FINAL DISPOSITION NOTICE SENT TO IB

06/10/2023

FIMP

FINAL DISPOSITION PROCESSED

06/10/2023

FICR

FINAL DISPOSITION NOTICE CREATED, TO BE SENT TO IB

04/10/2023

NRCC

NOTICE OF REGISTRATION CONFIRMATION EMAILED

04/07/2023

R.PR

REGISTERED-PRINCIPAL REGISTER

04/07/2023

LIME

LIMITATION FROM THE IB EXAMINED AND ENTERED

10/05/2023

GPNX

NOTIFICATION PROCESSED BY IB

25/04/2023

NPUB

OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED

18/04/2023

PUBO

PUBLISHED FOR OPPOSITION

18/04/2023

OPNS

NOTIFICATION OF POSSIBLE OPPOSITION SENT TO IB

05/04/2023

OP2R

NOTICE OF START OF OPPOSITION PERIOD CREATED, TO BE SENT TO IB

05/04/2023

NONP

NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED

29/03/2023

RFNT

REFUSAL PROCESSED BY IB

21/03/2023

CNSA

APPROVED FOR PUB - PRINCIPAL REGISTER

11/03/2023

TEME

TEAS/EMAIL CORRESPONDENCE ENTERED

07/03/2023

CRFA

CORRESPONDENCE RECEIVED IN LAW OFFICE

07/03/2023

TROA

TEAS RESPONSE TO OFFICE ACTION RECEIVED

07/03/2023

RFCS

NON-FINAL ACTION MAILED - REFUSAL SENT TO IB

27/02/2023

RFRR

REFUSAL PROCESSED BY MPU

27/02/2023

LIMG

LIMITATION OF GOODS RECEIVED FROM IB

13/02/2023

RFCR

NON-FINAL ACTION (IB REFUSAL) PREPARED FOR REVIEW

01/01/2023

CNRT

NON-FINAL ACTION WRITTEN

31/12/2022

DOCK

ASSIGNED TO EXAMINER

29/12/2022

MAFR

APPLICATION FILING RECEIPT MAILED

14/06/2022

NWOS

NEW APPLICATION OFFICE SUPPLIED DATA ENTERED

10/06/2022

REPR

SN ASSIGNED FOR SECT 66A APPL FROM IB

09/06/2022

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