KR20150016405A - 과체중 및 비만의 치료 방법 - Google Patents
과체중 및 비만의 치료 방법 Download PDFInfo
- Publication number
- KR20150016405A KR20150016405A KR1020157000155A KR20157000155A KR20150016405A KR 20150016405 A KR20150016405 A KR 20150016405A KR 1020157000155 A KR1020157000155 A KR 1020157000155A KR 20157000155 A KR20157000155 A KR 20157000155A KR 20150016405 A KR20150016405 A KR 20150016405A
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- bupropion
- management program
- naltrexone
- weight management
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Classifications
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H20/00—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
- G16H20/10—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
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Abstract
Description
Claims (35)
- 심혈관계 부작용의 위험이 증가된 과체중 또는 비만 대상체를 확인하는 단계; 및
상기 대상체에게 치료 유효량의 서방형 날트렉손, 또는 그의 약제학적으로 허용되는 염, 및 서방형 부프로피온, 또는 그의 약제학적으로 허용되는 염을 투여하는 단계를 포함하는, 과체중 또는 비만에서 심혈관계 부작용의 위험이 증가된 대상체의 치료 방법. - 청구항 1에 있어서, 상기 과체중 또는 비만 대상체는 상기 대상체가:
a) 상기 확인에 앞서 >3개월 전에 기록된 심근 경색의 병력;
관상 동맥 우회로 이식술, 스텐트 삽입술, 경피적 경혈관 관상동맥 형성술, 또는 레이저 죽종제거술(atherectomy)을 포함하는 관상 동맥 혈관 재건술의 병력;
경동맥 내막 절제술, 하지 아테롬성 동맥경화증 죽종제거술, 복부 대동맥 동맥류의 회복, 대퇴 또는 슬와 우회술을 포함하는 경동맥 또는 말초 혈관 재건술의 병력;
허혈성(ischemic) 변화, 등급화된 운동 부하 검사에서 ECG 변화, 또는 포지티브 심장 이미징 연구에 의한 협심증;
상기 확인되기 전 2년 이내에 간단한 촉진에 의해 평가되는 <0.9의 발목 상완 지수; 및
상기 확인되기 전 2년 이내에 관상 동맥, 경동맥, 또는 하지 동맥의 50% 이상 협착으로 구성된 군으로부터 선택된 적어도 하나의 위험 인자가 있는 심혈관계 질병에 걸린 것으로 진단받고/받거나
b) <145/95 mmHg에서 약물 요법에 의해 또는 약물 요법 없이 조절되는 고혈압;
약물 요법을 필요로 하는 이상지질혈증;
상기 확인되기 전 12개월 내에 여성들에서 <50 mg/dL 또는 남성들에서 <40 mg/dL으로 기록된 낮은 HDL 콜레스테롤; 및
현재 담배 흡연자로 구성된 군으로부터 선택된 적어도 2개의 위험 인자가 있는 제2형 당뇨병에 걸린 것으로 진단받은 경우에 심혈관계 부작용의 위험이 증가된 것으로 확인되는, 방법. - 청구항 1 또는 2에 있어서, 상기 대상체가 다음 2개의 순서들 중: 즉, 1주일 동안 하루에 한 번 서방형 날트렉손, 또는 그의 약제학적으로 허용되는 염, 및 서방형 부프로피온, 또는 그의 약제학적으로 허용되는 염을 포함하는 활성 연구 약물 치료에 이어 1주일 동안 하루에 한번 위약 치료; 또는 1주일 동안 위약 치료에 이어 1주일 동안 서방형 날트렉손, 또는 그의 약제학적으로 허용되는 염, 및 서방형 부프로피온, 또는 그의 약제학적으로 허용되는 염을 포함하는 활성 연구 약물 치료 중의 하나에 따른 치료를 받는 동안 도입 2주 기간을 추가로 포함하는, 방법.
- 청구항 1 내지 3 중의 어느 한 항에 있어서, 상기 대상체는:
상기 확인되기 전 3개월 이내에 심근 경색; 캐나다 심혈관 학회 등급 매김 방식에 의한 협심증 III 또는 IV 등급; 뇌졸중을 포함한 뇌혈관 질병의 임상 병력; 부비동 빈맥 이외의 빈박성 부정맥의 병력; 항고혈압제들에 의한 치료와 무관하게 ≥145/95 mmHg의 혈압; 상기 확인되기 전 3개월 내에 불안정한 체중; 계획된 비만대사 수술, 심장 수술, 또는 관상 동맥 혈관 성형술; 측정된 GFR이 <30 mL/분으로 정의된 중증 신장 장애; 간부전의 임상 병력 또는 문서로 기록된 정상 상한치의 3 배보다 더 큰 ALT 또는 AST; HIV 또는 간염으로 알려진 감염; 오피오이드류의 만성적 사용 또는 그에 대한 양성 선별; 상기 확인되기 전 6 개월 이내에 니코틴 의존을 예외로 하는 최근의 약물 또는 알코올 남용 또는 의존; 열성 경련, 두개 외상, 또는 대상체가 발작에 걸리기 쉽게 하는 다른 조건들을 포함하는 발작의 병력; 조증의 병력 또는 활성 정신병, 활성 폭식증 또는 신경성 식욕 부진이지만, 폭식 장애는 아닌 것으로 현재 진단받음; 자살 시도의 위험; 우울증의 새로운 발병 또는 증상의 급격한 악화를 포함하지만, 우울증에 대한 만성적 치료에 대해 안정한 대상체들을 포함하지 않는 급성 우울증 질환; 울혈성 심부전 NYHA 분류 3 또는 4 포함하여 4년 미만으로 예상되는 기대 수명을 갖는 임의의 조건; 흑색종이 아닌 피부암 또는 외과적으로 치료된 자궁 경부암을 포함하지 않는 이전 5년 이내의 악성 종양의 병력; 다른 부프로피온 또는 날트렉손 함유 제품의 현재 사용; 날트렉손 또는 부프로피온에 과민 반응 또는 불내증의 병력; 상기 확인되기 전 14일 이내에 모노아민 산화 효소 억제제들의 사용; 상기 확인되기 전 30일 내에 임의의 임상 시험용 약물, 장치 또는 절차의 사용; 임신하거나 또는 모유 수유 중인 여성, 또는 현재 임신하려는 여성, 또는 1년 이내에 1회의 월경기를 가진 폐경기 즈음의 여성 및 산아 제한을 실천하고자 하지 않는 여성을 포함하는 분만 가능한 여성; 및 광대역 인터넷에 일관성 있게 액세스할 수 있는 능력이 없음으로 구성된 군으로부터 선택된 한 가지 이상의 특징을 갖지 않는, 방법. - 과체중 또는 비만 대상체를 확인하는 단계; 및
웹-기반 체중 관리 프로그램, 전화-기반 체중 관리 프로그램, 또는 이들의 조합과 병용하여, 상기 대상체에게 치료 유효량의 서방형 날트렉손, 또는 그의 약제학적으로 허용되는 염, 및 서방형 부프로피온, 또는 그의 약제학적으로 허용되는 염을 투여하는 단계를 포함하는, 과체중 또는 비만의 대상체를 치료하는 방법. - 청구항 5에 있어서, 상기 확인된 대상체는 단순 비만으로 BMI가 ≥30 kg/m2 및 ≤45 kg/m2인, 방법.
- 청구항 5에 있어서, 상기 확인된 대상체는 이상지질혈증 및/또는 조절된 고혈압이 있고 BMI가 ≥27 kg/m2 및 ≤45 kg/m2인 방법.
- 청구항 5 내지 7 중의 어느 한 항에 있어서, 상기 대상체는:
제1형 또는 제2형 당뇨병 진단의 병력; 상기 확인되기 6개월 이내의 심근 경색; 캐나다 심혈관 학회 등급 매김 방식에 의한 협심증 III 또는 IV 등급; 허혈성 및 출혈성 뇌졸중을 포함하는 큰 혈관의 대뇌 피질 뇌졸중의 임상 병력; ≥145/95 mmHg의 혈압; 상기 확인되기 전 4주 이내에 지질 강하제들의 복용의 개시 또는 변경; 발작, 두개골 외상, 폭식증, 신경성 식욕 부진, 또는 상기 대상체가 발작에 걸리기 쉽게 하는 다른 조건들의 병력; 상기 확인되기 전 3개월 이내에 불안정한 체중; 체중 감량을 위해 의도된 처방된 또는 비처방(OTC) 약물의 사용, 또는 상기 확인되기 전 1개월 이내에 체중 감량 프로그램에 참여; 비만에 대해 계획된 수술적 또는 장치 개입; <30 mL/분/1.73 m2의 추정된 사구체 여과율(GFR)로 정의된 중증 신장 장애의 현재 또는 병력; 간부전의 임상 병력 또는 현재 문서로 기록된 정상 상한치의 >3배인 아스파르테이트 아미노 전이 효소 (AST) 또는 알라닌 아미노 전이 효소 (ALT); ≥126 ㎎/dL의 공복 혈당 또는 ≥400 ㎎/dL의 공복 트리글리세리드류; HIV 또는 간염으로 알려진 감염; 오피오이드류의 만성적 사용 또는 그에 대한 양성 선별; 상기 확인되기 전 6개월 내에 약물 또는 알코올 남용 또는 의존 또는 양성의 소변 약물 선별; 상기 확인되기 6개월 내의 담배 제품의 규칙적 사용 또는 니코틴 대체 제품의 사용; 조증의 병력 또는 활성 정신병으로 현재 진단받음; 자살 시도의 위험; 우울증의 새로운 발병 또는 증상의 급격한 악화를 포함하지만, 우울증에 대한 만성적 치료에 대해 안정한 대상체들을 포함하지 않는 급성 우울증 질환; 다른 부프로피온 또는 날트렉손 함유 제품들의 현재 사용; 날트렉손 또는 부프로피온에 대한 과민 반응 또는 불내증의 병력; 상기 확인되기 전 14일 이내에 항경련제, 도파민 효능제, 테오필린, 또는 경구용 코르티코 스테로이드 또는 모노아민 산화 효소 억제제의 현재 사용; 상기 확인되기 전 30일 이내에 임의의 임상 시험용 약물, 장치 또는 절차의 사용; 임신하거나 또는 모유 수유 중인 여성, 또는 현재 임신하려는 여성, 또는 1년 이내에 월경기를 가진 폐경기 즈음의 여성 및 산아 제한을 실천하고자 하지 않는 여성을 포함하는 분만 가능한 여성; 규칙적인 중간-강도의 운동을 수행할 능력이 없음 또는 내키지 않음; 및 이메일 사용 및 CLI 프로그램 액세스 시험을 완료할 능력이 없음으로 구성된 군으로부터 선택된 한 가지 이상의 특징들을 갖지 않는, 방법. - 청구항 1 내지 8 중의 어느 한 항에 있어서, 상기 대상체는 적어도 26주 동안 치료받는, 방법.
- 청구항 1 내지 9 중의 어느 한 항에 있어서, 상기 대상체에게 웹-기반 체중 관리 프로그램, 전화-기반 체중 관리 프로그램, 또는 이들의 병용을 제공하는 단계를 추가로 포함하는, 방법.
- 청구항 10에 있어서, 상기 전화-기반 체중 관리 프로그램은 상기 대상체에 대한 1회 이상의 코칭 통화(coaching call)를 포함하는, 방법.
- 청구항 10 또는 11에 있어서, 상기 전화-기반 체중 관리 프로그램은 하나 이상의 웹 코칭 도구를 임의로 포함하는 방법.
- 청구항 10 내지 12 중의 어느 한 항에 있어서, 상기 웹-기반 또는 전화-기반 체중 관리 프로그램은 상기 대상체에게 행동, 영양 또는 체력 단련 교육 중 한 가지 이상을 제공하는, 방법.
- 청구항 13에 있어서, 상기 교육은 훈련된 건강 또는 체력 단련 코치 및/또는 등록된 영양사에 의하여 제공되는, 방법.
- 청구항 14에 있어서, 상기 훈련된 건강 또는 체력 단련 코치 및/또는 상기 등록된 영양사는 상기 대상체에 대해 전화를 통해서 또는 웹사이트를 통해서 상기 대상체와 상담하고, 도움말 및 동기 부여 메시지들; 질문과 답변을 통한 코칭; 웹사이트를 통한 상기 대상체의 문의들에 대한 실시간 응답을 위한 주간 근무 시간; 주간 교육 자료; 비디오 레슨; 배지 보상으로 추적되는 체중, 운동, 또는 식이요법; 목표 설정; 진행 추적; 및 상기 대상체가 체중 관리 프로그램에 참여하도록 장려하는 의사소통으로 구성된 군으로부터 선택된 한 가지 이상의 주제를 제공하는 방법.
- 청구항 10 내지 15 중의 어느 한 항에 있어서, 상기 체중 관리 프로그램은 새로운 행동, 영양 및/또는 체력 단련 교육 테마 및 2개 이상의 목표를 매주 도입하는 단계; 상기 새로운 테마 및 목표와 관련된 정보 내용 및/또는 비디오 레슨을 매주 제공하는 단계; 및 상기 훈련된 건강 또는 체력 단련 코치의 한 개 이상의 동기 부여 메시지를 상기 대상체에게 주중 1일 이상 제공하는 단계를 포함하는, 방법.
- 청구항 10 내지 16 중의 어느 한 항에 있어서, 상기 체중 관리 프로그램은 상기 훈련된 건강 또는 체력 단련 코치가 상기 대상체에게 실시간 질문과 답변 반응들에 대한 일정을 제공하는 단계를 포함하는, 방법.
- 청구항 10 내지 17 중의 어느 한 항에 있어서, 상기 체중 관리 프로그램은 상기 대상체의 체중의 매주 기록, 상기 대상체의 음식 섭취량의 매일 기록, 및 상기 대상체의 활동의 매일 기록의 군으로부터 선택된 한 가지 이상의 활동들을 포함하는, 방법.
- 청구항 10 내지 18 중의 어느 한 항에 있어서, 상기 체중 관리 프로그램은 상기 대상체가 상기 대상체의 음식 섭취량을 기록하는 단계를 포함하고, 상기 프로그램은 특정 음식 및/또는 식사에 대한 칼로리의 컴퓨터 데이터베이스를 사용하여 상기 기록된 음식 섭취량에 대한 칼로리를 추적할 수 있는, 방법.
- 청구항 10 내지 19 중의 어느 한 항에 있어서, 상기 웹-기반 체중 관리 프로그램은 상기 대상체가 특정 프로그램 목표를 달성하는 경우 상기 대상체를 배지들로 보상하는 단계를 포함하는, 방법.
- 청구항 10 내지 20 중의 어느 한 항에 있어서, 상기 체중 관리 프로그램은 상기 대상체에게 체중 감량 진행의 그래프 표시를 제공하는 단계를 포함하는, 방법.
- 청구항 10 내지 21 중의 어느 한 항에 있어서, 상기 대상체는 체중 관리 프로그램의 일부로서 기록되는 체중 감량 목표를 설정하는, 방법.
- 청구항 10 내지 22 중의 어느 한 항에 있어서, 상기 체중 관리 프로그램은 상기 대상체에게 스트레칭 및 걷기 또는 다른 가벼운 심혈관계 활동에 대한 지침을 제공하는 단계를 포함하는, 방법.
- 청구항 10 내지 23 중의 어느 한 항에 있어서, 상기 체중 관리 프로그램은 스트레칭을 수행하고 운동 활동하는 방법을 보여주는 비디오 클립들을 제공하는 단계를 포함하는, 방법.
- 청구항 10 내지 24 중의 어느 한 항에 있어서, 상기 체중 관리 프로그램은 상기 대상체가 기록한 운동 및 활동 로그(log)에 근거하여 상기 대상체가 소모한 칼로리를 추적하는 단계를 포함하는, 방법.
- 청구항 10 내지 25 중의 어느 한 항에 있어서, 상기 체중 관리 프로그램은 적어도 26, 52 또는 78주의 기간을 갖는, 방법.
- 청구항 1 내지 26 중의 어느 한 항에 있어서, 32 mg/일의 서방형 날트렉손, 또는 그의 약제학적으로 허용되는 염, 및 360 mg/일의 서방형 부프로피온, 또는 그의 약제학적으로 허용되는 염을 상기 대상체에게 투여하는, 방법.
- 청구항 1 내지 27 중의 어느 한 항에 있어서, 상기 대상체에게 8 mg의 서방형 날트렉손 및 90 mg의 서방형 부프로피온을 함유하는 정제 중에서 상기 서방형 날트렉손, 또는 그의 약제학적으로 허용되는 염, 및 상기 서방형 부프로피온, 또는 그의 약제학적으로 허용되는 염을 투여하는, 방법.
- 청구항 1 내지 28 중의 어느 한 항에 있어서, 날트렉손 및 부프로피온으로의 상기 치료는 상기 대상체의 심혈관계 부작용의 위험을 증가시키지 않는, 방법.
- 청구항 1 내지 29 중의 어느 한 항에 있어서, 날트렉손 및 부프로피온으로의 상기 치료는 상기 대상체의 심혈관계 부작용의 위험을 감소시키는, 방법.
- 청구항 1 내지 30 중의 어느 한 항에 있어서, 상기 심혈관계 부작용이 심혈관계 사망, 치명적이지 않은 심근 경색, 또는 치명적이지 않은 뇌졸중인, 방법.
- 청구항 1 내지 31 중의 어느 한 항에 있어서, 상기 대상체는 적어도 5%, 10% 또는 15%의 체중 감량의 백분율을 달성하는, 방법.
- 청구항 1 내지 32 중의 어느 한 항에 있어서, 상기 대상체는 체중 관리 프로그램의 일부로서 직접(in-person) 상담을 받지 않는, 방법.
- 청구항 1 내지 32 중의 어느 한 항에 있어서, 상기 대상체는 체중 관리 프로그램의 일부로서 5회 초과의 직접(in-person) 상담 세션을 받지 않는, 방법.
- 청구항 1 내지 32 중의 어느 한 항에 있어서, 상기 대상체는 체중 감량을 위한 집중 행동 수정 (BMOD) 프로그램을 받지 않는, 방법.
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