首页
登录
职称英语
Without fanfare or legislation, the government is orchestrating a quiet revo
Without fanfare or legislation, the government is orchestrating a quiet revo
游客
2025-04-16
17
管理
问题
Without fanfare or legislation, the government is orchestrating a quiet revolution in how it regulates new medicines. The revolution is based on the idea that the sicker people are, the more freedom they should have to try drugs that are not yet fully tested. For fifty years government policy has been driven by another idea: the fear that insufficiently tested medicines could cause deaths and injuries. The urgent needs of people infected with HIV, the AIDS virus, and the possibility of meeting them with new drugs have created a compelling countervailing force to the continuing concern with safety. As a result, government rules and practices have begun to change. Each step is controversial. But the shift has already gone far beyond AIDS. New ways are emerging for very sick people to try some experimental drugs before they are marketed. People with the most serious forms of heart disease, cancer, emphysema, Alzheimer’ s or Parkinson’ s disease, multiple sclerosis, epilepsy, diabetes, or other grave illnesses can request such drugs through their doctors and are likelier to get them than they would have been four years ago. "We’ve been too rigid in not making lifesaving drugs available to people who otherwise face certain death," says Representative Henry Waxman, of California, who heads the subcommittee that considers changes in drug-approval policies. "It’s true of AIDS, but it’s also true of cancer and other life- threatening diseases."
For the first time, desperate patients have become a potent political force for making new medicines available quickly. People with AIDS and their advocates, younger and angrier than most heart-disease or cancer patients, are drawing on two decades of gay activists’ success in organizing to get what they want from politicians. At times they found themselves allied with Reagan Administration deregulators, scientists, industry representatives, FDA staff members, and sympathetic members of Congress. They organized their own clinical trials and searched out promising drugs here and abroad. The result is a familiar Washington story: a crisis—AIDS—helped crystallize an informal coalition for reform.
AIDS gave new power to old complaints. As early as the 1970s the drug industry and some independent authorities worried that the Food and Do, g Administration’ s testing requirements were so demanding that new drugs were being unreasonably delayed. Beginning in 1972, several studies indicated that the United States had lost its lead in marketing new medicines and that breakthrough drugs—those that show new promise in treating serious or life-threatening diseases— had come to be available much sooner in other countries. Two high-level commissions urged the early release of breakthrough drugs. So did the Carter Administration, but the legislation it pro- posed died in Congress. Complaints were compounded by growing concern that "if we didn’t streamline policies, red tape wot, Id be an obstacle to the development of the biotechnology revolution," as Frank E. Young, who was the head of the FDA from 1984 to 1989, put it in an interview with me.
Young was a key figure in the overhaul of the FDA’s policies. A pioneer in biotechnology and a former dean of the University of Rochester’s medical school, he came to Washington with an agenda and headed the agency for five and a half years—longer than anyone else has since the 1960s. Young took the FDA job to help introduce new medicines created by biotechnology-- whose promise he had seen in his own gene-cloning lab--and to get experimental medicines to desperately iii people more quickly. He had seen people die waiting for new medicines because "they were in the wrong place at the wrong time," he said. That is now changing. [br] According to the passage, patients who are gravely ill ______.
选项
A、can get experimental drugs more quickly than ever before
B、are still unable to get experimental drugs because of government strict policies
C、can’t afford some expensive experimental drugs
D、refuse to be treated with experimental drugs
答案
A
解析
转载请注明原文地址:https://tihaiku.com/zcyy/4040651.html
相关试题推荐
Governmentisaninstitutionresultingfromman’sgroupwayoflifewhichma
Governmentisaninstitutionresultingfromman’sgroupwayoflifewhichma
Governmentisaninstitutionresultingfromman’sgroupwayoflifewhichma
Therewasagroupofdemonstrators______anti-governmentslogansinthesquare.A、
Businessandgovernmentleadersconsidertheinflationratetobeanimporta
Businessandgovernmentleadersconsidertheinflationratetobeanimporta
Businessandgovernmentleadersconsidertheinflationratetobeanimporta
Businessandgovernmentleadersconsidertheinflationratetobeanimporta
Businessandgovernmentmanagersoftenpromote"cleandesk"policiestoavoiddi
Noformofgovernmentintheworldis______;eachsystemreflectsthehistoryan
随机试题
ABesidekillingandBeatingprairiedogs,theferretoccupiesCitsvictim’sDhom
Tosavemoney,heoftenbuyssome(use)________books.used空格处位于限定词some和名词books之间
1.题目:人教版九年级下册《浓硫酸的腐蚀性和稀释》片段教学 2.内容 3
Semantictriangleismadeupofreferenc
列表试述中枢性瘫痪与周围性瘫痪的鉴别要点。
双侧髂脊最高点的连线平对( )A.第3腰椎棘突 B.第4腰椎棘突 C.第5
根据核算主体的不同,以下不属于会计报表分类的是()。A:企业会计报表 B:上市
(2020年真题)标准差是一组数据分散程度的一种度量,是表示精确度的重要指标。在
2012年4月27日,甲在乙经营的小吃店吃完一碗10元的米粉后,出现食物中毒,花
某新建项目,建设期为3年,共向银行借款1300万元,其中第1年借款700万元,第
最新回复
(
0
)