H einz Edgar Lehmann, a pioneer of psychopharmacology, was born in Berlin, Germany on July 17, 1911, graduated from the University of Berlin in 1935, emigrated to Canada in 1937, fleeing from Nazi Germany, and took a post at the Verdun Protestant Hospital (Montreal's Douglas Hospital) as a junior psychiatrist. 1 In 1944, he published among other interesting papers, an article on the use of massive doses of nicotinic acid in the treatment of posttraumatic confusional state. 2 In 1947, he was appointed Clinical Director of the Verdun Protestant Hospital where he remained affiliated for 60 years. 1 In 1948, he became a naturalized Canadian citizen and he was hired as an assistant professor at McGill, later attaining the rank for full professor. In 1949, he developed a hypnotic with a short half-life made of scopolamine, apomorphine, phenobarbital, hexobarbital, and nicotinic acid. 1,2 From 1970 to 1974, he was Chair of the Department of Psychiatry at McGill University, and he published more than 300 articles, mostly on psychopharmacology. 3,4 In the spring of 1953, Lehmann was seeking a new treatment for his more severely disturbed patients, when a Rhône-Poulenc representative gave him a copy of Delay and Deniker's article about a new compound for treatment of psychosis 5 not specifically schizophrenia, encouraging him and Gorman Hanrahan, to use this compound later called chlorpromazine on a series of psychotic patients. Lehmann read the first article of Delay and Deniker about Chlorpromazine at home in his bathtub 4 and found his curiosity arrested and with Gorman E. Hanrahan conducted their first trial with this new drug. 6 In February 1954, Heinz Lehmann published the first clinical article on the use of chlorpromazine 6 in Canada. Chlorpromazine was the first synthetic drug used to control states of mania and psychomotor excitement, marking the birth of modern psychopharmacology, and Lehmann gave a full clinical description of what we now call its antipsychotic effects. This groundbreaking clinical observation was responsible for turning chlorpromazine into the first neuroleptic medication in history, hailed as the first "antipsychotic" medication. 1,3 Chlorpromazine reduces the intensity of psychotic symptoms, reducing schizophrenia positive symptoms, such as delusion and hallucinations. It gained attention worldwide because of its safety, becoming a more humane treatment option, which permanently reshaped the landscape of psychiatry for both psychotic patients and psychiatrists. 1,3 After the arrival of chlorpromazine, which affects among others the dopamine 2 receptor, many institutionalized patients could finally leave psychiatric hospitals and return to their families, communities, and continue treatment as an outpatient. This discovery was a revolution in the treatment of psychotic disorders that has spawned at least 2 subsequent generations of antipsychotic medications and contributed to the emptying of huge chronic psychiatric hospitals and contributed to the growth of community mental health treatmen...