Thalidomide () was introduced as a sedative drug in the late 1950s that was typically used to cure morning sickness. In 1961, it was withdrawn due to teratogenicity and neuropathy. There is now a growing clinical interest in thalidomide, and it is introduced as an immunomodulatory agent used primarily in combination with dexamethasone to treat multiple myeloma. The drug is a potent teratogen in zebrafish, chickens, rabbits and primates, including humans: severe birth defects may result if the drug is taken during pregnancy.

Thalidomide was sold in a number of countries across the world from 1957 until 1961 when it was withdrawn from the market after being found to be a cause of birth defects in what has been called "one of the biggest medical tragedies of modern times". It is not known exactly how many worldwide victims of the drug there have been, although estimates range from 10,000 to 20,000. Thalidomide has since been found to be a viable treatment for a number of medical conditions. It is being prescribed again in a number of countries, although its use remains controversial, including its testing in the developing world. The thalidomide tragedy led to much stricter testing being required for drugs and pesticides before they can be licensed.

History

Development

Thalidomide was developed by German pharmaceutical company Grünenthal in Stolberg (Rhineland) near Aachen, although others challenge this claim. A report published by Martin W. Johnson, director of the Thalidomide Trust in the United Kingdom, mentioned evidence found by Argentinian author Carlos De Napoli that suggested the drug had been first developed as a possible antidote to nerve toxins, such as Sarin, by Otto Ambros, a Nazi scientist who joined Grünenthal after the war. Correspondence between various drug companies -- French firm Rhône-Poulenc, which was under Nazi control during the war years, Astra AB, which held the Swedish licence to distribute thalidomide, and IG Farben, the German pharmaceutical firm -- seem to confirm the existence of the product years before Grünenthal secured a patent in 1954. Furthermore, a relation has been suggested between testing thalidomide and the Nazi death camps. Grünenthal has responded to these claims by stating, "To our knowledge there was no collaboration between Grünenthal and Rhône-Poulenc for the development of Contergan/thalidomide. Three Grünenthal employees discovered thalidomide and Grünenthal is the sole inventor on the patent." According to Grünenthal, Dr. Heinrich Mückter was one of those responsible for inventing Thalidomide. Other sources mark Dr. Mückter as a fledgling pharmacologist who carried out wartime experiments on Polish prisoners to find a cure for typhus, causing the death of hundreds in the process.

De Napoli suggested elsewhere that thalidomide may have been first synthesised by British scientists at the University of Nottingham in 1949. Thalidomide, launched by Grünenthal on 1 October 1957, was found to act as an effective tranquilizer and painkiller and was proclaimed a "wonder drug" for insomnia, coughs, colds and headaches. It was also found to be an effective antiemetic which had an inhibitory effect on morning sickness, and so thousands of pregnant women took the drug to relieve their symptoms. At the time of the drug's development scientists did not believe any drug taken by a pregnant woman could pass across the placental barrier and harm the developing foetus. The Food and Drug Administration of the United States never licensed thalidomide for general use; according to Time Magazine, "In the half dozen reported U.S. cases of birth malformations due to thalidomide, the drug was obtained from abroad." However, samples had been distributed to a number of physicians as part of a clinical trial, in which 20,000 patients in the US received thalidomide.

Birth defects

In the late 1950s and early 1960s, more than 10,000 children in 46 countries were born with deformities such as phocomelia as a consequence of thalidomide use. The Australian obstetrician William McBride and the German pediatrician Widukind Lenz suspected a link between birth defects and the drug, a theory Lenz proved in 1961. McBride was later awarded a number of honours, including a medal and prize money by the prestigious L'Institut de la Vie in Paris.

In the United Kingdom the drug was licensed in 1958. Of the approximately 2,000 babies born with defects, 466 survived. The drug was withdrawn in 1961. In 1968, after a long campaign by ''The Sunday Times'' newspaper, a compensation settlement for the UK victims was reached with Distillers Company Limited (now part of Diageo). This compensation, which is distributed by the Thalidomide Trust in the UK, was substantially increased by Diageo in 2005. The UK Government gave survivors a grant of £20 million, to be distributed through the Thalidomide Trust, in December 2009. In Germany approximately 2,500 thalidomide babies were born.

In the United States, pharmacologist and M.D. Frances Oldham Kelsey refused Food and Drug Administration (FDA) approval for an application from the Richardson-Merrell company to market thalidomide, saying further studies were needed, which reduced the impact of thalidomide in United States patients. Although thalidomide was never approved for sale in the United States, millions of tablets had been distributed to physicians during a clinical testing program. It was impossible to know how many pregnant women had been given the drug to help alleviate morning sickness or as a sedative.

Canada was the last country to stop the sales of the drug, in early 1962.

In 1962, the United States Congress enacted laws requiring tests for safety during pregnancy before a drug can receive approval for sale in the U.S. Other countries enacted similar legislation, and thalidomide was not prescribed or sold for decades.

In September 2010, as noted in an article titled "The Public's Quiet Savior From Harmful Medicine", the FDA honored Dr. Kelsey with the first Kelsey award. The award, given annually to a FDA staff member, came 50 years after Dr. Kelsey, then a new medical officer at the agency, first reviewed the application from the William S. Merrell Company of Cincinnati.

Mechanism

Researchers soon discovered that only one particular optical isomer of thalidomide caused the teratogenicity. The pair of enantiomers, while mirror images of each other, cause different effects, although it is now known that the "safe" isomer can be converted to the teratogenic isomer once in the human body.(see ''Teratogenic mechanism'').

Revived interest

In 1964 Jacob Sheskin, Professor at the Hebrew University of Jerusalem at Hadassah University Hospital and the chief staff and manager of Hansen Leper Hospital in Jerusalem, administered thalidomide to a critically ill patient with erythema nodosum leprosum (ENL), a painful complication of leprosy, in an attempt to relieve his pain in spite of the ban. The patient slept for hours, and was able to get out of bed without aid upon awakening. The result was followed by more favorable experiences and then by a clinical trial. Sheskin found that patients with erythema nodosum leprosum, a painful skin condition, experienced pain relief when taking thalidomide.

Further work conducted in 1991 by Dr. Gilla Kaplan at Rockefeller University in New York City showed that thalidomide worked in leprosy by inhibiting tumor necrosis factor alpha. Kaplan believed thalidomide could be an effective treatment for AIDS. He partnered with Celgene Corporation to further develop the potential for thalidomide in AIDS and tuberculosis. However, clinical trials for AIDS proved disappointing.

In 1994, Dr. Robert D'Amato at Harvard Medical School discovered thalidomide was a potent inhibitor of new blood vessel growth (known as angiogenesis). Numerous cancer clinical trials for thalidomide began based upon this finding. In 1997, Dr. Bart Barlogie reported thalidomide's initial effectiveness against Multiple Myeloma, and thalidomide was later approved in the United States by the FDA for use in this malignancy. The FDA has also approved the drug's use in the treatment of erythema nodosum leprosum. There are studies underway to determine the drug's effects on arachnoiditis and several types of cancers. However, physicians and patients alike must go through a special process, known as S.T.E.P.S., to prescribe and receive thalidomide, to ensure no more children are born with birth defects traceable to the medication. Celgene Corporation has also developed analogues to thalidomide, such as lenalidomide, that are substantially more powerful and have fewer side effects — except for greater myelosuppression.

More recently the World Health Organisation (WHO) has stated that:

"The WHO does not recommend the use of thalidomide in leprosy as experience has shown that it is virtually impossible to develop and implement a fool-proof surveillance mechanism to combat misuse of the drug. The drug clofazimine is now a component of the multidrug therapy (MDT), introduced by WHO in 1981 as the standard treatment for leprosy and now supplied free of charge to all patients worldwide."

United States

On July 16, 1998, the FDA approved the use of thalidomide for the treatment of lesions associated with Erythema Nodosum Leprosum (ENL). Because of thalidomide's potential for causing birth defects, the drug may be distributed only under tightly controlled conditions. The FDA required that Celgene Corporation, which planned to market thalidomide under the brand name ''Thalomid'', establish a System for Thalidomide Education and Prescribing Safety (S.T.E.P.S.) oversight program. The conditions required under the program include limiting prescription and dispensing rights only to authorized prescribers and pharmacies, keeping a registry of all patients prescribed thalidomide, providing extensive patient education about the risks associated with the drug, and providing periodic pregnancy tests for women who take the drug. On May 26, 2006, the U.S. Food and Drug Administration granted accelerated approval for thalidomide (Thalomid, Celgene Corporation) in combination with dexamethasone for the treatment of newly diagnosed multiple myeloma (MM) patients. The FDA approval came seven years after the first reports of efficacy in the medical literature and Celgene took advantage of "off-label" marketing opportunities to promote the drug in advance of its FDA approval for the myeloma indication. Thalomid, as the drug is commercially known, sold over $300 million per year, while only approved for leprosy.

United Kingdom

Thalidomide is available to only a small number of patients in the UK, generally in specialist cancer treatment centres where research trials are taking place and where specialist doctors have experience in its use.

Brazil

Brazil has the second highest prevalence rate of leprosy in the world, and thalidomide has been used by Brazilian physicians as the drug of choice for the treatment of severe ENL since 1965. A study published in 1996 reported 33 people born in Brazil after 1965 with thalidomide embryopathy. Since 1994 the production, dispensing, and prescription of thalidomide have been strictly controlled, but cases of thalidomide embryopathy continue.

Possible indications

Serious infections including sepsis and tuberculosis cause the level of Tumor necrosis factor-alpha (TNFα) to rise. TNFα is a chemical mediator in the body, and may enhance the wasting process in cancer patients as well. Thalidomide may reduce the levels of TNFα, and it is possible that the drug's effect on ENL is caused by this mechanism.

Thalidomide also has potent anti-inflammatory effects that may help ENL patients. In July 1998, the FDA approved the application of Celgene to distribute thalidomide under the brand name Thalomid for treatment of ENL. Pharmion Corporation, who licensed the rights to market thalidomide in Europe, Australia, and various other territories from Celgene, received approval for its use against multiple myeloma in Australia and New Zealand in 2003. Thalomid, in conjunction with dexamethasone, is now standard therapy for multiple myeloma.

Thalidomide is also prescribed for its anti-inflammatory effects in actinic prurigo, an autoimmune skin disease. Thalidomide has been used in chronic bullous dermatosis of childhood (CBDC) with encouraging results. Peripheral neuritis may be a limiting factor for long term use of thalidomide.

Thalidomide also inhibits the growth of new blood vessels (angiogenesis), which may be useful in treating macular degeneration and other diseases. This effect helps AIDS patients with Kaposi's sarcoma, although there are better and cheaper drugs to treat the condition. Thalidomide may be able to fight painful, debilitating aphthous lesions in the mouth and esophagus of AIDS patients which prevent them from eating. The FDA formed a Thalidomide Working Group in 1994 to provide consistency between its divisions, with particular emphasis on safety monitoring. The agency also imposed severe restrictions on the distribution of Thalomid through the System for Thalidomide Education and Prescribing Safety (STEPS) program.

Thalidomide is also being investigated for treating symptoms of prostate cancer, glioblastoma, lymphoma, arachnoiditis, Behçet's disease, and Crohn's disease. In a small trial, Australian researchers found thalidomide caused a doubling of the number of T cells in patients, allowing the patients' own immune system to attack cancer cells.

Studies carried out in animal models have suggested that the use of combined therapy with thalidomide and glucantime could have a therapeutic benefit in the treatment of Visceral Leshmaniasis.

A study published in April 2010 discusses the ability of thalidomide to induce vessel maturation, which may be useful as a therapeutic strategy for the treatment of vascular malformations. The research was conducted in an experimental model of the genetic disease hereditary hemorrhagic telangiectasia.

Thalidomide and multiple myeloma

Thalidomide was first tested in humans as a single agent for the treatment of multiple myeloma in 1996 due to its antiangiogenic activity. The New England Journal of Medicine published the full study in 1999. Since then, many studies have shown that thalidomide, in combination with dexamethasone, has increased the survival of multiple myeloma patients. The combination of thalidomide and dexamethasone, often in combination with melphalan, is now one of the most common regimens for patients with newly diagnosed multiple myeloma, with an improved response rate of up to 60-70%. Thalidomide may also cause side effects such as polyneuropathy, fatigue, skin rash, and venous thromboembolism (VTE), or blood clots, which could lead to stroke or myocardial infarction. Bennett et al. have conducted a systematic review of VTE associated with thalidomide in multiple myeloma patients. They have found that when thalidomide was administered without prophylaxis, VTE rates reached as high as 26%. Owing to the high rates of VTE associated with thalidomide in combination with dexamethasone or doxorubicin, a black box warning was added in the US in 2006 to the package insert for thalidomide, indicating that patients with multiple myeloma who receive thalidomide-dexamethasone may benefit from concurrent thromboembolism prophylaxis or aspirin. In addition, owing to these side effects, newer drugs, such as bortezomib (marketed as Velcade) and a thalidomide derivative, lenalidomide (marketed as Revlimid), have increased in popularity.

Teratogenic mechanism

Thalidomide is racemic – it contains both left- and right-handed isomers in equal amounts. The (''R'') enantiomer is effective against morning sickness but the (''S'') is teratogenic. The enantiomers can interconvert (racemize) ''in vivo'' – that is, if a human is given pure (''R'')-thalidomide or (''S'')-thalidomide, both isomers will later be found in the serum – therefore, administering only one enantiomer will not prevent the teratogenic effect.

The mechanism of thalidomide's teratogenic action has led to over 2000 research papers and the proposal of fifteen or sixteen plausible mechanisms. A theoretical synthesis in 2000 suggested the following mechanism: thalidomide intercalates (inserts itself) into DNA in G-C (guanine-cytosine) rich regions. Owing to its glutarimide part, (S) thalidomide fits neatly into the major groove of DNA at purine sites. Such intercalation impacts upon the promoter regions of the genes controlling the development of limbs, ears, and eyes such as IGF-I and FGF-2. These normally activate the production of the cell surface attachment integrin αvβ3 with the resulting αvβ3 integrin dimer stimulating angiogenesis in developing limb buds. This then promotes the outgrowth of the bud (IGF-I and FGF-2 are also both known to stimulate angiogenesis). Therefore, by inhibiting the chain of events, thalidomide causes the truncation of limb development. In 2009 this theory received strong support, with research showing "conclusively that loss of newly formed blood vessels is the primary cause of thalidomide teratogenesis, and developing limbs are particularly susceptible because of their relatively immature, highly angiogenic vessel network."

Inactivation of the protein cereblon

Thalidomide binds to and inactivates the protein cereblon, which is important in limb formation. The inactivation leads to a teratogenic effect on fetal development. This was confirmed when the scientists, using genetic techniques, reduced the production of cereblon in developing chick embryo and zebrafish embryo. These embryos had defects similar to those treated with thalidomide. While the mechanism that causes teratogenicity has been established, the mechanism for other therapeutic effects remains unclear.

Thalidomide analogs

The exploration of the antiangiogenic and immunomodulatory activities of thalidomide has led to the study and creation of thalidomide analogs. In 2005, Celgene received FDA approval for lenalidomide (Revlimid) as the first commercially useful derivative. Revlimid is only available in a restricted distribution setting to avoid its use during pregnancy. Further studies are being conducted to find safer compounds with useful qualities. Another analog, pomalidomide, is in the clinical trial phase. These thalidomide analogs can be used to treat different diseases, or used in a regimen to fight two conditions.

Notable people affected

Rock Brynner, son of Yul Brynner, author of ''Dark Remedy'', who took Thalidomide as an adult for his immune disorder.

Mat Fraser, musician, actor and performance artist born with phocomelia of both arms.

Alvin Law, radio broadcaster, born without arms.

Louise Medus Mansell, daughter of David Mason, campaigner for increased compensation for thalidomide children, born with no arms or legs.

Tony Meléndez, award winning singer and guitarist who plays with his feet, known internationally due to the recognition received from Pope John Paul II and U.S. President Ronald Reagan.

Thomas Quasthoff, an internationally acclaimed bass-baritone who describes himself: "1.34 meters tall, short arms, seven fingers — four right, three left — large, relatively well formed head, brown eyes, distinctive lips; profession: singer." Niko von Glasow produced a documentary called ''Nobody's perfect'', based on the lives of 12 people affected by the drug, which was released in 2008.

Terry Wiles, born with phocomelia of both arms and legs, who has become known internationally through the television drama ''On Giant's Shoulders'' and the best-selling book of the same name.

References

Further reading

External links

Thalidomide monograph from Chemical and Engineering News. (Archived by WebCite® at http://www.webcitation.org/5nWHyOCfI)

Thalidomide product monograph (Needs registration)

Multiple Myeloma Research Foundation article on Thalidomide

International Myeloma Foundation article on Thalidomide

Thalidomide — Annotated List of Links (covering English and German pages)

WHO Pharmaceuticals Newsletter No. 2, 2003 - See page 11, Feature Article

Grünenthal GmbH — Thalidomide

Celgene website on Thalomid

The Return of Thalidomide — BBC

CBC Digital Archives – Thalidomide: Bitter Pills, Broken Promises

Thalidomide UK

The Thalidomide Trust

The International Contergan Thalidomide Alliance website

"The Big Pitch: How would you conduct a campaign for the new Thalidomide Drugs?", forum of pharmaceutical and medical marketing professionals commenting on how they would address the thalidomine controversies.

Category:Teratogens Category:Carcinogens Category:Health disasters Category:Leprosy Category:German inventions Category:Withdrawn drugs Category:Immunosuppressants Category:Phthalimides Category:Glutarimides

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Coordinates	53°25′″N18°26′″N
name	Harold Matthew Evans
birth date	June 28, 1928
birth place	Newton Heath, Manchester, United Kingdom
education	Durham University
occupation	Journalist, Editor
spouse	Tina Brown
children	George, Izzy
nationality	British, American
credits	''The Sunday Times''''The Week Magazine''''The Guardian''BBC Radio 4 }}

Sir Harold Matthew Evans (born 28 June 1928) is a British-born journalist and writer who was editor of ''The Sunday Times'' from 1967 to 1981. He has written various books on history and journalism. Since 2001, Evans has served as editor-at-large of ''The Week Magazine'' and since 2005, he has been a contributor to ''The Guardian'' and BBC Radio 4.

On June 13th 2011 Sir Harold Evans was appointed editor-at-large of the ''Reuters'' news agency.

Personal life

Evans was born to Welsh parents in Newton Heath, Manchester, where he attended Brookdale High School Newton Heath with the future Alfred, Lord Morris of Manchester, who nicknamed him "Poshie" because he was the only boy in the school whose father - a railway driver - owned an automobile.

Early career

Evans began his career as a reporter for a weekly newspaper in Ashton-under-Lyne, Lancashire at 16 years old. After completing his national service in the Royal Air Force, he entered Durham University where he graduated with honours in politics and economics and subsequently earned a Master of Arts degree for a thesis on foreign policy. He became an assistant editor of the ''Manchester Evening News'' and won a Harkness Fellowship in 1956-57 for travel and study in the United States. He began to gain a reputation on his return from the U.S. when he was appointed editor of the regional daily ''The Northern Echo'', where one of his campaigns resulted in a national programme for the detection of cervical cancer.

The Sunday Times

During his 14-year tenure as editor of the ''Sunday Times'', Evans was responsible for its crusading style of investigative reporting, which brought to public attention many stories and scandals that were officially denied or ignored.

One such report was about the plight of hundreds of British Thalidomide children who had never had any compensation for severe birth defects some had suffered. This turned into a campaign for the newspaper's ''Insight'' investigative team, and Evans himself took on the drug companies responsible for the manufacture of Thalidomide, pursuing them through the English courts and eventually gaining victory in the European Court of Human Rights. As a result, the victims' families won compensation after more than a decade. Moreover, the British Government was compelled to change the law inhibiting the reporting of civil cases.

Other influential investigative reports included the exposure of Kim Philby as a Soviet spy and the publication of the diaries of former Labour Minister Richard Crossman, thereby risking prosecution under the Official Secrets Act.

When Rupert Murdoch acquired Times Newspapers Limited in 1981, Evans was appointed editor of ''The Times''. However, he remained with the paper only a year, resigning over policy differences relating to editorial independence. Evans wrote an account in a book entitled ''Good Times, Bad Times'' (1984). On leaving ''The Times'', Evans became director of Goldcrest Films and Television.

Move to America

In 1984, Evans moved to the United States, where he taught at Duke University. He was subsequently appointed editor-in-chief of ''The Atlantic Monthly Press'' and became editorial director of ''US News and World Report''. In 1986 he was the founding editor of ''Conde Nast Traveler'', dedicated to "truth in travel".

Evans was appointed president and publisher of Random House trade group from 1990 to 1997 and editorial director and vice chairman of ''US News and World Report'', the ''New York Daily News'', and ''The Atlantic Monthly'' from 1997 to January 2000, when he resigned to concentrate on writing.

Evans's best-known work, ''The American Century'', won critical accaim when it was published in 1998. The sequel, ''They Made America'' (2004), described the lives of some of the country's most important inventors and innovators. ''Fortune'' identified it as one of the best books in the 75 years of that magazine's publication. It was adapted as a four-part television mini-series that same year and as a National Public Radio special in the USA in 2005.

Harold Evans became an American citizen in 1993, and lives in New York with his wife Tina Brown and their two children. In 2000 he was named one of International Press Institute's 50 ''Heroes of World Press Freedom''. He was knighted for services to journalism in 2004.

On June 13th 2011, he became Editor at Large at Reuters.

Works

Radio and Television programs

BBC Radio 4 - A Point of View 13-week series from 29 July 2005

Love letter to America BBC News, 29 July 2005

BBC audio interview 16 May 2005

They Made America PBS

Bibliography

''Editing and Design: A Five-Volume Manual of English, Typography and Layout'' (1972) ISBN 0-434-90550-X

''Essential English for Journalists, Editors and Writers'' (1972) ISBN 0-7126-6447-5

''Newspaper Design'' (1973) ISBN 0-434-90554-2

''Editing and Design'' (1974) ISBN 0-434-90552-6

''Handling Newspaper Text'' (1974) ISBN 0-03-012041-1

''News Headlines'' (1974) ISBN 0-03-007501-7

''Front Page History: Events of Our Century That Shook the World'' (1984) ISBN 0-88162-051-3

''Good Times, Bad Times'' (1984) ISBN 0-689-11465-6 Also earlier edition of ''Good Times, Bad Times''. Includes sections of black-and-white photographic plates, plus a few charts and diagrams in text pages

''Editing and Design: Book 2: Handling Newspaper Text'' (1986) ISBN 0-434-90548-8

''Assignments: The Press Photographers' Association Yearbook (Assignments)'' (1988) by Harold Evans (commentary), Anna Tait (editor) ISBN 0-7148-2501-8

''Makers of Photographic History'' (1990) ISBN 0-948489-09-X

''Eyewitness 2: 3 Decades Through World Press Photos'' (1992) ISBN 0-907621-55-4

''Pictures on a Page: Photo-Journalism, Graphics and Picture Editing'' (1997) ISBN 0-7126-7388-1

''The American Century'' (1998) ISBN 0-679-41070-8

''War of Words: Memoirs of a South African Journalist'' (2000) by Benjamin Pogrund, Harold Evans ISBN 1-888363-71-1

''Shots in the Dark: True Crime Pictures'' (2001) by Gail Buckland, Harold Evans ISBN 0-8212-2775-0

''The Best American Magazine Writing 2001'' (2001) Harold Evans (editor) ISBN 1-58648-088-X

''The BBC Reports: On America, Its Allies and Enemies, and the Counterattack on Terrorism'' (2002) ISBN 1-58567-299-8

''Best American Magazine Writing 2002'' (2002) ISBN 1-58648-137-1

''War Stories: Reporting in the Time of Conflict from the Crimea to Iraq'' (2003) ISBN 1-59373-005-5

''They Made America: Two Centuries of Innovators from the Steam Engine to the Search Engine'' (2004) ISBN 0-316-27766-5

''We the People'' (2007) ISBN 0-316-27717-7

''My Paper Chase: True Stories of Vanished Times'' (2009) ISBN 978-0-316-03142-4

Footnotes

External links

Sir Harold Evans official website

Column archive at ''The Daily Beast''

Column archive at the ''Huffington Post''

Column archive at ''The Guardian''

Harold Evans at ''The Daily Beast''

;Interviews

Harold Evans: They Made America from ''Bill Thompson's Eye on Books'', audio of Harold Evans interview

The American Century' from ''CNN Book News'', 13 November 1998, includes audio clips from Harold Evans

Interview with Evans about ''The American Century'' from ''Booknotes'', 7 February 1999

The American Century transcript of Harold Evans interview from ''PBS NewsHour'', 8 June 1999

Media Giants: Harry Evans profile on ''Media Circus'', July 2007

Harold Evans Sees Bright Future for Print-on-Demand Newspapers from ''PBS MediaShift'', 29 October 2009, interview includes audio clips

Reuters Editor-at-Large Harry Evans interviews former Secretary of State Henry Kissinger and 2012 Republican presidential candidate Jon Huntsman, ''Reuters'' on YouTube, 14 June 2011

Category:Alumni of Durham University Category:American journalists Category:British foreign policy writers Category:English historians Category:English journalists Category:English newspaper editors Category:Duke University faculty Category:English expatriates in the United States Category:Foreign policy writers Category:The Guardian journalists Category:Harkness Fellows Category:Knights Bachelor Category:Naturalized citizens of the United States Category:People from Newton Heath Category:The Sunday Times people Category:The Times people Category:1928 births Category:Living people