This past October marked the 41st anniversary of one of biotechnology’s and American medicine’s most significant milestones: the U.S. Food and Drug Administration’s approval of human insulin synthesized in genetically engineered bacteria to treat diabetes. The first “biopharmaceutical”—a drug made with molecular genetic engineering techniques—to be approved, it launched a revolutionary era in drug development.

Insulin is secreted in the pancreas and is essential to the metabolism of carbohydrates and fats. Insulin deficiency leads to the development of diabetes. Many diabetics require regular injections of insulin to maintain life and health.

As the FDA medical reviewer and head of the evaluation team for “Humulin” (the brand name of the human insulin), I had a front‐​row seat to this landmark event. The saga is remarkable in several ways, not least of which is that, although both the drugmakers and regulators were exploring unknown territory, the development of the drug and its regulatory review progressed smoothly and rapidly.

Miracle drug / Insulin in crude form was first produced a century ago, in 1922, by Canadian researchers Frederick Banting and Charles Best. Their work lifted the death sentence that had previously been imposed on diabetics. By the end of that year, drug company Eli Lilly had devised a method for much higher purification. But this miracle drug was dependent on extracting insulin from the pancreases of pigs and cows, using waste products from the meat packing industry. More than two tons of pig parts were needed to extract just 8 oz. of purified insulin.

Over the next half century, the pig and cow‐​derived insulins, which differ slightly in chemical composition from human insulin, were constantly improved in purity and formulated in ways that offered physicians and diabetic patients greater control over blood sugar. The extracted insulin was a miracle drug.

By the early 1970s, however, a crisis emerged. The supply of animal pancreases declined and the prevalence of insulin‐​requiring diabetes grew, leading to widespread fears of possible future shortages of insulin. Fortunately, around the same time, a new and powerful tool—recombinant DNA technology, also known as “genetic engineering” or “gene-splicing”—became available, offering the promise of unlimited amounts of insulin that, unlike the insulin from animals, was identical to the molecule produced in the human body.

The seminal molecular genetic engineering experiment wasreported in a 1973 research articleby academic scientists Stanley Cohen, Herbert Boyer, and their collaborators. They isolated a ringlet of DNA called a “plasmid” from a bacterium, used certain enzymes to splice a gene from another bacterium into the plasmid, and introduced the resulting “recombinant,” or chimeric, DNA intoE. colibacteria. When these now “recombinant” bacteria reproduced, the plasmids containing the foreign DNA were likewise propagated and produced amplified amounts of the functional recombinant DNA. And because DNA contains the genetic code that directs the synthesis of proteins, this new methodology promised the ability to induce genetically modified bacteria (or other cells) to synthesize desired proteins in large amounts.

Scientists at Eli Lilly immediately saw the promise of this technology to produce unlimited quantities of human insulin in bacteria. After obtaining the recombinantE. colibacteria that synthesized human insulin from biotech startup Genentech, they developed processes for the large‐​scale cultivation of the organism (in huge fermenters like those used to make wine or beer) and for the purification and formulation of the drug.

Insulins had long been Lilly’s flagship products, and the company’s expertise was evident in the purification, laboratory testing, and clinical trials of human insulin. The company’s scientists painstakingly verified that their product was extremely pure and identical to pancreatic human insulin.

Lilly began clinical trials of its human insulin in July 1980. The product performed superbly. There were no systematic problems with treating “naive” patients (who had never received injections of insulin) or those who switched from animal to human insulin. Moreover, a small number of patients who had had adverse reactions to the animal insulins tolerated the human insulin well.

FDA review / The New Drug Application, the dossier that provided evidence of the synthetic insulin’s safety and efficacy, was submitted in May 1982 to the FDA, where I was the medical reviewer and head of the evaluation team. Over many years, the FDA had had extensive experience with insulins and with drugs derived from various microorganisms, so it was decided that no fundamentally new regulatory paradigms were needed to evaluate the recombinant human insulin. In other words, recombinant DNA techniques were viewed as an extension, or refinement, of long‐​used and familiar methods for making drugs. That proved to be a historic, precedent‐​setting, and correct decision.

Based on my team’s exhaustive review of Lilly’s data, which were obtained from pre‐​clinical testing in animals and later in clinical trials involving thousands of diabetics, the FDA granted marketing approval for human insulin in October 1982. The review and approval took only five months when the agency’s average approval time for new drugs was 30.5 months.

In retrospect, that rapid approval was particularly remarkable for a drug that was produced with a revolutionary new technology and that would be available in pharmacies nationwide to millions of American diabetics.

Bureaucratic mindset / The back story, however, is revealing. My team and I were ready to recommend approvalafterfour months’ review. But when I took the packet to my supervisor, he said: “Four months? No way! If anything goes wrong with this product down the road, people will say we rushed it, and we’ll be toast.”

That’s the bureaucratic mindset. I don’t know how long he would have delayed it, but when he went on vacation a month later, I took the packet to his boss, the division director, and he signed off.

That anecdote is an example of Milton Friedman’s observation that to understand the motivation of an individual or organization, you need to “follow the self‐​interest.” A large part of regulators’ self‐​interest lies in staying out of trouble. One way to do that, my supervisor understood, is not to approve in record time a product that might experience unanticipated problems.

The Humulin approval had significant effects. An October 30, 1982, New York Timesfront‐​page articlequoted me predicting that the speedy approval was a major step forward in the “scientific and commercial viability” of recombinant DNA technology. “We have now come of age,” I said, and potential investors and entrepreneurs agreed. Seeing that biopharmaceuticals would compete with other medicines on a level playing field, the “biotechnology industry” was on the fast track.

Unfortunately, the rapid approval of human insulin proved to be an anomaly. Even with a toolbox of improved technologies available to both the FDA and industry, bringing a new drug to market on average now takes 10–12 years and costs more than $2.5 billion. There hasn’t even been much improvement in review times from the pre‐​electronic era when New Drug Applications were submitted in paper form.

Regulators are highly risk‐​averse, few new drugs are approved without convening extramural advisory committees, and decisions are sometimes hijacked by political forces outside the FDA. Even so, five of the highest‐​revenue U.S. drugs in 2022 were produced by biotechnology, either with recombinant DNA or monoclonal antibody technology.

Other FDA‐​regulated biotech sectors have fared much worse. Regulators have made a colossal mess of the regulation of genetically engineered animals, which the FDA bizarrely chose to regulate as “new animal drugs” based on their interpretation of a 1938 law. That byzantine process led to a grotesquely prolonged, 20‐​plus‐​year review of a faster‐​growing Atlantic salmon.(See “Regulators Kept a Fish Treading Water for Years,” Fall 2021.)

More disarray occurred with genetically engineered mosquitoes to control mosquitoes that carry viral diseases. Inexplicably, it took the FDA more than five years to decide that, for regulatory purposes, this “gene drive” technology was a form of pesticide, and that jurisdiction over its approval belonged at the U.S. Environmental Protection Agency. As a result of this bureaucratic bungling, the entire biotech sector of genetically engineered animals is moribund. (See “How the FDA Virtually Destroyed an Entire Sector of Biotechnology,” Winter 2017–2018.)

Government regulation has not aged as gracefully as genetic engineering technology itself, which has advanced significantly over the years. Regulators are supposed to abide by the “contract” that society has made with them: civil servants are granted lifetime tenure and are protected from political pressure and retaliation, in return for which they are supposed to make decisions based solely on the public interest. But often they do not​.To get FDA‐​regulated products to those who need them, congressional oversight must emerge from hibernation and create a healthier, more constructive balance.