Kadcyla - Top-Selling Antibody Drug Conjugate (ADC) (2024)

Kadcyla (ado-trastuzumab emtansine, T-DM1), a second-generation antibody-drug conjugate (ADC), is the most commercially successful ADC. In 2021, the global ADC market exceeded $5.2 billion, with Kadcyla sales reaching $2.17 billion.

Kadcyla was first approved by the U.S. Food and Drug Administration (FDA) in 2013, for patients with HER2-positive, late-stage (metastatic) breast cancer. It is the first ADC approved for solid tumors.

Introduction of Kadcyla

Kadcyla is a HER2-targeted antibody-drug conjugate that contains the humanized anti-HER2 IgG1, trastuzumab, covalently linked to the microtubule inhibitor DM1 (a maytansine derivative) via the stable thioether linker MCC (4-[N-maleimidomethyl] cyclohexane-1-carboxylate). An average of 3.5 DM1 molecules are conjugated to each molecule of trastuzumab.

Kadcyla - Top-Selling Antibody Drug Conjugate (ADC) (1)

Figure 1. Structure of Kadcyla, source: reference [5]

DM1 is a maytansine derivative. Maytansine, first isolated from the bark of African shrub Maytenus ovatus in 1972, is a potent microtubule-targeted compound that induces mitotic arrest and kills tumor cells at sub-nanomolar concentrations. Therefore, this class of cytotoxic drugs also belongs to the class of microtubule protein inhibitors, and the two most commonly used in ADCs today are DM1 and DM4.

Clinical Efficacy and Market Performance of Kadcyla

The latest FDA approval in 2019 was based on KATHERINE (NCT01772472), a randomized, multicenter, open-label trial of 1486 patients with HER2-positive EBC who had residual invasive disease in the breast and/or axillary lymph nodes following neoadjuvant treatment with taxane + trastuzumab-based therapy.

The primary objective of the KATHERINE study is to evaluate, the effectiveness and safety of adjuvant treatment with Kadcyla versus trastuzumab in patients after surgery.

The primary endpoint of the study is invasive disease-free survival (IDFS), which is the time from randomization grouping to recurrence of invasive breast cancer or death from any cause. Secondary endpoints included disease-free survival (DFS) and overall survival (OS).

Patients were grouped 1:1 and received Kadcyla or Herceptin (trastuzumab), respectively, as well as radiation and/or hormonal therapy according to local treatment guidelines. At a median follow-up time of 40 months, patients in the Kadcyla group had a statistically significant improvement in IDFS compared to the Herceptin group and a 50% reduction in the risk of death or recurrence of invasive disease. At 3 years, 88.3% of patients in the Kadcyla group were relapse-free compared to 77.0% in the Herceptin group.

Kadcyla - Top-Selling Antibody Drug Conjugate (ADC) (2)

Figure 2. Efficacy Results from KATHERINE
Kadcyla - Top-Selling Antibody Drug Conjugate (ADC) (3)

Figure 3. 3-year iDFS rates were 88.3% for KADCYLA vs 77.0% for Herceptin, references [1]

The most common adverse reactions (ADRs) (≥25%) included nausea, fatigue, skeletal muscle pain, bleeding, headache, elevated transaminases, thrombocytopenia, and peripheral neuropathy, with most ADRs being mild to moderate grade 1 or 2 ADRs and the incidence of severe ADRs >0.5%.

In 2021, Kadcyla had global sales of $2.18 billion, ranking as the most commercially successful ADC. According to an ADC market size report by Nature Reviews Drug Discovery, sales of Kadcyla are expected to be $2.3 billion in 2026, indicating limited room for future growth.

Kadcyla - Top-Selling Antibody Drug Conjugate (ADC) (4)
Figure 4. Sales of ADC drugs

There are 2 main reasons for its limited room for future growth, one is the high pricing of Kadcyla. The pricing of Kadcyla in USA is $3,709 /100mg, $5,929/160mg, which limits the use of the drug for some patients.

On the other hand, biosimilars are coming to market one after another, further eroding Kadcyla's share. In India, an analogue, Ujvira, has been approved for 20% of the price of Kadcyla. ADCs with the same target, HER2, are also being developed and commercialized, undoubtedly posing a threat to Kadcyla.

Kadcyla (T-DM1) Compared to DS-8201 & RC48

Globally, two ADC products targeting HER2 have been launched: Enhertu (DS-8201) by Daiichi Sankyo and Disitamab Vedotin (RC48) by RemeGen Co.

Kadcyla - Top-Selling Antibody Drug Conjugate (ADC) (5)

Figure 5. Kadcyla (T-DM1) Compared to DS-8201 & RC48, source: reference [3]

1.Trastuzumab Deruxtecan(Enhertu,T-DXd,DS-8201)

  • ▶Company: Daiichi Sankyo / AstraZeneca
  • Target: HER2
  • Antibody: Humanized IgG1 monoclonal antibody Trastuzumab
  • Drug/payload: DXd (topoisomerase)
  • Linker: GFLG (tetrapeptide)
  • Indications: Breast cancer, gastric cancer, lung cancer, etc.
  • Status: Available in 2019

Enhertu consists of an anti-HER2 antibody, Trastuzumab, coupled to the cytotoxic drug DXd via a linker, GFLG. The linker is a cleavable tetrapeptidyl linker (Gly-Phe-Leu-Gly (GFLG)), which is not only stable but also can be specifically cleaved and has a strong cell membrane permeability, allowing it to exert a "bystander effect".

Kadcyla - Top-Selling Antibody Drug Conjugate (ADC) (6)

Figure 6. Structure of Enhertu. Source: reference [2]

The cytotoxic drug employs DXd, a new DNA topoisomerase inhibitor that improves the hydrophobic properties of the drug, allowing each antibody to be loaded with 7 or 8 DXd molecules. The high DAR allows the efficacy of Enhertu to be considered 2 to 4 times higher than previously approved marketed ADC drugs.

Enhertu was first approved for marketing in the United States in 2019 for the treatment of HER2-positive metastatic breast cancer.

2. Disitamab Vedotin (Aidixi, RC48)

  • Company: RemeGen Co.
  • Target: HER2
  • Antibody: recombinant humanized IgG1 monoclonal antibody Hertuzumab
  • Drug/Payload: Duocarmycin / Seco-DUBA
  • Linker: MC-Val-Cit-PAB
  • Indication: Gastric cancer
  • Status: Available in 2021

Disitamab Vedotin, consists of a recombinant humanized HER2 IgG1 monoclonal antibody coupled to MMAE via a cleavable linker. It is indicated for the treatment of patients with locally advanced or metastatic HER2 overexpressing gastric cancer, including adenocarcinoma of the gastroesophageal junction, who have received at least 2 systemic chemotherapies.

Kadcyla - Top-Selling Antibody Drug Conjugate (ADC) (7)

Figure 7. Structure of Disitamab Vedotin, source: Reference [3]

In June 2021, the National Medical Products Administration (NMPA) granted conditional approval for Disitamab Vedotin.

As a novel agent, RC48 as monotherapy or adjuvant treatment in clinical practice for the therapy of other cancer in the world, including UC, biliary tract cancer (BTC), non-small cell lung cancer (NSCLC), and HER2+ and HER2-low expressing BC.

Anti-Her2 ADCs in Clinical Trials

Except for the three anti-Her2 ADC approved for marketing, there are more than 20 ADCs have entered clinical testing. Among them, trastuzumab duocarmazine (SYD985) making the best progress.

Kadcyla - Top-Selling Antibody Drug Conjugate (ADC) (8)
Figure 8. List of anti-Her2 ADCs in clinical trials or on the market, source: reference [4]

Trastuzumab Duocarmazine (SYD985)

  • Company: Byondis
  • Target: HER2
  • Antibody: Monoclonal antibody trastuzumab
  • Drug/Payload: MMAE (monomethyl auristatin E)
  • Linker: vc-seco-DUBA
  • Indication: Breast Cancer, Endometrial cancer
  • Status: Phase III

SYD985 is an investigational next-generation HER2 ADC that was previously granted Fast Track Designation by the FDA in January 2018. In addition, its U.S. marketing application was accepted by the FDA on July 12, 2022, with a PDUFA date set for May 12, 2023.

SYD985 consists of the monoclonal antibody trastuzumab and a cleavable linker-drug called valine-citrulline-seco-DUocarmycin-hydroxyBenzamide-Azaindole (vc-seco-DUBA). which is designed using Byondis' proprietary ByonZine technology platform - - duocarmazine linker drug technology.

Kadcyla - Top-Selling Antibody Drug Conjugate (ADC) (9)

Figure 9. SYD985 formula, anti-HER2 trastuzumab conjugated to seco-DUBA via a cleavable linker sensitive to cathepsin B. Source: reference [5]

On July 18, 2022, Byondis announced that the European Medicines Agency (EMA) has validated the Marketing Authorization Application (MAA) for SYD985 in patients with HER2-positive unresectable locally advanced or metastatic breast cancer (MBC).

The MAA for SYD985 is based on data from the pivotal phase III TULIP. The trial was a randomized, multicenter, open-label clinical trial (n=436) comparing the efficacy of SYD985 with physician's choice (PC) for the treatment of patients with HER2-positive unresectable locally advanced or metastatic breast cancer. The primary endpoint is progression-free survival (PFS).

Byondis presented preliminary results from TULIP3 at the ESMO 2021 Congress. The results showed that SYD985 significantly improved PFS in patients with HER2-positive unresectable locally advanced or metastatic breast cancer, with a PFS of 7.0 months in the SYD985 group and 4.9 months in the PC group. In addition, the overall survival (OS) in the group receiving SYD985 showed a trend of improvement with an HR of 0.83.

Biopharma PEG providesGMP standard PEG derivativesand bulk orders via custom synthesis, offering the opportunity to match customers' special quality requirements.ADC linkerswith molecular weights, branching, and functional groups not listed in our online catalog may be available by custom synthesis.

References:
[1] https://www.kadcyla-hcp.com/early-breast-cancer/efficacy/clinical-trial-results.html
[2] Nakada T, Sugihara K, Jikoh T, Abe Y, Agatsuma T. The Latest Research and Development into the Antibody-Drug Conjugate, [fam-] Trastuzumab Deruxtecan (DS-8201a), for HER2 Cancer Therapy.Chem Pharm Bull (Tokyo). 2019;67(3):173-185. doi:10.1248/cpb.c18-00744
[3] Shi F, Liu Y, Zhou X, Shen P, Xue R, Zhang M. Disitamab vedotin: a novel antibody-drug conjugates for cancer therapy. Drug Deliv. 2022 Dec;29(1):1335-1344. doi: 10.1080/10717544.2022.2069883. PMID: 35506447; PMCID: PMC9090390.
[4] Zhang X, Huang AC, Chen F, Chen H, Li L, Kong N, Luo W, Fang J. Novel development strategies and challenges for anti-Her2 antibody-drug conjugates. Antib Ther. 2022 Jan 27;5(1):18-29. doi: 10.1093/abt/tbac001. PMID: 35146330; PMCID: PMC8826051.
[5] Joubert, N.; Beck, A.; Dumontet, C.; Denevault-Sabourin, C. Antibody–Drug Conjugates: The Last Decade. Pharmaceuticals 2020, 13, 245. https://doi.org/10.3390/ph13090245

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Kadcyla - Top-Selling Antibody Drug Conjugate (ADC) (2024)

FAQs

What is the best selling ADC drug? ›

Kadcyla (ado-trastuzumab emtansine, T-DM1), a second-generation antibody-drug conjugate (ADC), is the most commercially successful ADC.

What antibody-drug conjugates KADCYLA? ›

Ado-trastuzumab emtansine also known as T-DM1 (Kadcyla®; Genentech/Roche) is a human epidermal growth factor receptor 2 (HER2) antibody-drug conjugate that comprises the humanized anti-HER2 IgG1 (antibody) trastuzumab linked to the anti-mitotic agent mertansine (a maytansine derivative; also known as the maytansinoid ...

What is ADC antibody-drug conjugation? ›

Antibody-drug conjugates (ADC) are antibodies (mAbs) engineered to utilize the capability of monoclonal antibodies by combining them to cytotoxic agents. An ideal ADC has the following features: A monoclonal antibody (mAb) that targets a specific cancer antigen while not harming healthy cells.

What drugs are in the ADC market? ›

Commercial products
DrugTrade nameMaker
Trastuzumab emtansineKadcylaGenentech, Roche
Inotuzumab ozogamicinBesponsaPfizer/Wyeth
Polatuzumab vedotinPolivyGenentech, Roche
Enfortumab vedotinPadcevAstellas/Seattle Genetics
8 more rows

How many FDA approved ADCs are there? ›

Tubulin polymerization promoters target at the β-subunits of tubulin dimer to perturb microtubule growth, and they are exemplified by auristatin derivatives monomethyl auristatin E (MMAE) and monomethyl auristatin F (MMAF). Among the 14 approved ADC drugs, 5 of them use MMAE/MMAF as the payloads.

What is the highest selling drug in the US? ›

Humira was the top medicine in the United States based on sales in 2021, generating 17.3 billion U.S. dollars in revenue. The branded drug – used to treat, for example, arthritis – has topped revenue rankings for a number of years and made around 7.5 billion U.S. dollars more than second ranked Keytruda.

What is the chemo drug in Kadcyla? ›

Kadcyla is a combination of Herceptin and the chemotherapy medicine emtansine. Doctors call Kadcyla an antibody-drug conjugate targeted therapy. The emtansine is attached (conjugated) to the Herceptin.

Is Kadcyla stronger than Herceptin? ›

Kadcyla Not Better Than Standard of Care as First Treatment for Advanced-Stage, HER2-Positive Disease, but Causes Fewer Side Effects. Kadcyla wasn't more effective than Herceptin plus a taxane chemotherapy as the first treatment for advanced-stage, HER2-positive breast cancer, but offered women better quality of life.

Is Kadcyla same as T-DM1? ›

Trastuzumab emtansine is a type of targeted cancer drug. It is also known by its brand name Kadcyla and TDM1.

What is ADC drug antibody ratio? ›

Drug-to-antibody ratio (DAR) is the average number of drugs conjugated to the antibodies, which is an important attribute of ADCs. The DAR value affects the efficacy of the drug, as low drug loading reduces the potency, while high drug loading can negatively affect pharmaco*kinetics (PK)1 and toxicity.

What are ADC conjugation methods? ›

Antibody drug conjugates (ADCs) are synthesized by conjugating a cytotoxic drug or “payload” to a monoclonal antibody. The payloads are conjugated using amino or sulfhydryl specific linkers that react with lysines or cysteines on the antibody surface.

Why is antibody conjugation important? ›

Why conjugate your primary antibody? Due to their specificity, antibodies are widely used to detect and quantify antigens in numerous applications such as flow cytometry, ELISA, western blotting, immunohistochemistry, and lateral flow.

Which is the most widely used ADC? ›

The most common types of ADCs are flash, successive approximation, and sigma-delta.

Is ADC an immunotherapy? ›

ADCs interact with cancer and immune cells by eliciting mechanisms such as immunogenic cell death, antibody-dependent cell-mediated cytotoxicity and dendritic cell activation, ultimately providing potential synergism with immunotherapy.

Is ADC a chemotherapy? ›

ADCs are able to allow for much stronger doses of drugs than traditional chemotherapy because ADCs have less of an impact on healthy cells by carrying their payloads directly to the cancerous cells.

What are the approved ADC for oncology? ›

As of May 2021, the U.S. Food and Drug Administration (FDA) has approved ten ADCs, namely Adcetris®, Kadcyla®, Besponsa®, Mylotarg®, Polivy®, Padcev®, Enhertu®, Trodelvy®, Blenrep®, and Zynlonta™ as monotherapy or combinational therapy for breast cancer, urothelial cancer, myeloma, acute leukemia, and lymphoma.

What is the first approved ADC? ›

The first FDA-approved ADC (Food and drug administration approval) was gemtuzumab ozogamicin in 2000, for the treatment of acute myeloid leukemia. However, it was later withdrawn due to safety concerns. Despite challenges, several other ADCs have been approved for the treatment of various cancers.

What is the first approved antibody-drug conjugate? ›

Over 80 years following Ehrlich's fundamental realization, and supported by the successful development of chemotherapy in the 1940s and monoclonal antibodies (mAbs) in the 1970s, in 1983 the first successful antibody-drug conjugate (ADC) human clinical trial began using an anti-carcinoembryonic antibody tethered to ...

What is the largest selling drug in the world? ›

First to authorization in the U.S. and first to a full approval, the partners' mRNA-based COVID-19 shot has eclipsed AbbVie's Humira as the world's best-selling drug—and it's poised for an encore in 2022.

What is the most expensive drug in the world? ›

The Food and Drug Administration approved late last year CSL Behring's hemophilia B gene therapy Hemgenix, a one-off infusion that costs $3.5 million a dose, making it the world's most expensive drug.

Which medication is considered #1 in terms of total lifetime sales? ›

#1: Lipitor

The figure is a well-secured sales record. The drug was approved in the United States in 1997, but almost wasn't.

How successful is Kadcyla? ›

Three years after people started the study: Eighty-eight percent of the 743 people who received KADCYLA were still cancer free, compared to 77% of the 743 people who received Herceptin. The chance of cancer coming back was lowered by 50% for people who received KADCYLA compared to people who received Herceptin.

What is the advantage of Kadcyla? ›

If you have metastatic breast cancer, Kadcyla may help your cancer stop growing and spreading. (Metastatic breast cancer is cancer that's spread from the breast to other parts of the body.) It may also help you live longer.

What is the alternative to Kadcyla? ›

Enhertu Dramatically More Effective Than Kadcyla as Second Treatment for Metastatic HER2-Positive Breast Cancer. Enhertu more than doubled the 12-month progression-free survival rate than Kadcyla in people diagnosed with metastatic HER2-positive breast cancer that had been previously treated. Sep 21, 2021.

How long can you stay on Kadcyla? ›

KADCYLA is given for 14 cycles in early breast cancer

For HER2+ early breast cancer, KADCYLA is given every 3 weeks for 14 rounds of infusion—sometimes called "cycles"—unless the cancer comes back or side effects cause the treatment to be stopped sooner. Treatment with KADCYLA typically would last less than a year.

What is the recurrence rate of Kadcyla? ›

Recurrences: The study suggests that trastuzumab emtansine can lower the likelihood that the cancer will return (recurrences): About 13 out of 100 people who were given trastuzumab emtansine had a recurrence, compared to about 23 out of 100 people who received trastuzumab.

How much does Kadcyla cost in the US? ›

The cost for Kadcyla intravenous powder for injection 100 mg is around $3,950 for a supply of 1 powder for injection, depending on the pharmacy you visit. Quoted prices are for cash-paying customers and are not valid with insurance plans.

What are the long term side effects of Kadcyla? ›

Long-term side effects reported with Kadcyla include: serious liver problems,* such as liver damage. serious heart problems,* such as heart failure. nerve damage.

What foods should you avoid while taking Kadcyla? ›

Notes for Consumers: Do not drink grapefruit juice or eat grapefruit without talking to your health care professional while you are receiving Ado-Trastuzumab Emtansine. Side effects from Ado-Trastuzumab Emtansine may get worse.

What is the life expectancy of T-DM1? ›

Again, T-DM1 proved superior; patients receiving T-DM1 had a median overall survival of 22.7 months, compared with 15.8 months for patients receiving other third-line therapy.

What is ideal ADC? ›

An ideal ADC has an ENOB equal to its resolution. ADCs are chosen to match the bandwidth and required SNR of the signal to be digitized. If an ADC operates at a sampling rate greater than twice the bandwidth of the signal, then per the Nyquist–Shannon sampling theorem, near perfect reconstruction is possible.

What is ADC value range? ›

The ADC range is the maximum and minimum ADC input (e.g., 0 to +3.3V). The ADC resolution is the smallest distinguishable change in input (e.g., 3.3V/4095, which is about 0.81 mV). The resolution is the change in input that causes the digital output to change by 1.

What is efficacy of ADC? ›

Clinical efficacy of ADCs is determined by fine-tuning combination of tumor antigen, targeting antibody, cytotoxic payload and conjugation strategy (a). ADC binds to tumor target cell surface antigens (b) leading to trigger a specific receptor mediated internalization (c).

What are the three most common types of ADC? ›

Main types of ADC converters

Dual Slope ADC. Pipelined ADC. Flash ADC.

What are the two types of ADC? ›

Types of ADCs and Their Characteristics
ADC typeSample rateTypical resolution
Successive approximationModerate (~100 MHz)Moderate
PipelinedFast (~1 GHz)Low
Dual-slopeLowest (<1 kHz)High
FlashFastest (~10 GHz)Lowest
1 more row

What are the side effects of ADC? ›

The most common therapeutic-related adverse events of any grade were peripheral sensory neuropathy (42%), nausea (35%), fatigue (34%), neutropenia (19%), diarrhea (18%), pyrexia (14%), vomiting (13%), arthralgia (12%), pruritus (12%), myalgia (11%), peripheral motor neuropathy (11%), and alopecia (10%).

What is an ADC in oncology? ›

A substance made up of a monoclonal antibody chemically linked to a drug. The monoclonal antibody binds to specific proteins or receptors found on certain types of cells, including cancer cells. The linked drug enters these cells and kills them without harming other cells. Some ADCs are used to treat cancer.

What is an example of an antibody conjugate? ›

One example is trastuzumab emtansine (Kadcyla®), an antibody–drug conjugate incorporating the HER2-targeted antitumor properties of trastuzumab with the cytotoxic activity of the microtubule-inhibitory agent DM1.

Why is conjugation bad for us? ›

Thus, conjugation can spread antibiotic resistance quickly between bacteria of the microbiome and pathogens when selective pressure (antibiotics) is introduced.

Which ADC has the highest accuracy? ›

Dual slope integration type ADC has the highest accuracy.

Which best type of ADC is the fastest type of ADC? ›

A flash type ADC produces an equivalent digital output for a corresponding analog input in no time. Hence, flash type ADC is the fastest ADC. The 3-bit flash type ADC consists of a voltage divider network, 7 comparators and a priority encoder.

What is ADC also known as? ›

An analog-to-digital converter (also known as an ADC or an A/D converter) is an electronic circuit that measures a real-world signal (such as temperature, pressure, acceleration, and speed) and converts it to a digital representation of the signal.

Is Kadcyla an ADC? ›

Kadcyla (ado-trastuzumab emtansine, T-DM1), a second-generation antibody-drug conjugate (ADC), is the most commercially successful ADC.

Is ADC is a targeted therapy? ›

Antibody-drug conjugates (ADCs) are targeted therapies with the expectation of broadened therapeutic window due to tumor-specific drug delivery.

What is anti-HER2 ADC? ›

An antibody-drug conjugate (ADC) composed of a bispecific antibody against the extracellular domain of human epidermal growth factor receptor 2 (HER2; ERBB2) comprised of the single-chain variable fragment (scFv) of the anti-HER2 monoclonal antibody trastuzumab, which binds to domain IV of HER2, fused to the heavy ...

Are antibody-drug conjugates considered chemotherapy? ›

Antibody-drug conjugates or ADCs are a class of biopharmaceutical drugs designed as a targeted therapy for treating cancer. Unlike chemotherapy, ADCs are intended to target and kill tumor cells while sparing healthy cells. As of 2019, some 56 pharmaceutical companies were developing ADCs.

What are the side effects of antibody-drug conjugates? ›

The most common adverse events overall were lymphopenia (too few white blood cells), nausea, neutropenia (too few neutrophils), vision blurriness, and peripheral neuropathy.

What class of drugs are ADC? ›

Antibody-drug conjugates (ADCs) are a class of drugs designed as a targeted therapy for treating disease, but at the moment are widely used for the management or treatment of cancer [1]. They are complex molecules consisting of an antibody linked to a biologically active cytotoxic payload or drug [2].

What is the number one drug sold? ›

First to authorization in the U.S. and first to a full approval, the partners' mRNA-based COVID-19 shot has eclipsed AbbVie's Humira as the world's best-selling drug—and it's poised for an encore in 2022.

What is the full form of ADC drug? ›

Antibody-drug conjugates or ADCs are a new class of highly potent biopharmaceutical drug composed of an antibody linked, via a chemical linker, to a biologically active drug or cytotoxic compound.

What are the biggest blockbuster drugs of all time? ›

Common blockbuster drugs are Vioxx, Lipitor, and Zoloft. Blockbuster drugs are used for common ailments, such as diabetes, cholesterol, high blood pressure, and cancer, that many individuals face.

What is the peak sales of Enhertu? ›

Based on the large patient population, Jefferies analyst Naoya Miura has pegged Enhertu's risk-adjusted peak sales in the DESTINY-Breast04 third-line patient group at 151 billion Japanese yen ($1.31 billion).

What is the biggest selling drug in 2023? ›

Leading drugs worldwide based on projected 2023 sales (in billion U.S. dollars)
Drug name (company name)Projected sales in billion U.S. dollars
Keytruda (Merck & Co.)24
Comimaty/Covid-19 vaccine (Pfizer)19
Humira (AbbVie)13.5
Paxlovid (Pfizer)13
6 more rows
Jan 18, 2023

Which drug is the king of drugs? ›

Thus, the correct answer is option (A), 'Opium'.

What is the best selling drug in 2023? ›

Keytruda appears to be poised to reclaim the crown as the best-selling drug in 2023.

What is ADC in chemotherapy? ›

Unlike conventional chemotherapy treatments, which can damage healthy cells, antibody drug conjugates (ADCs) are targeted medicines that deliver chemotherapy agents to cancer cells. 1 ADCs deliver the chemotherapy via a linker attached to a monoclonal antibody that binds to a specific target expressed on cancer cells.

What drug has saved the most lives? ›

Penicillin (1942)

It is estimated that Penicillin has saved between 80 million and 200 million lives and without its discovery and implementation, 75% of people today would not be alive because their ancestors would have succumbed to infection.

What is the most important drug ever made? ›

Penicillin. Discovered in 1928 and put to use to cure infections in 1942, this is arguably the most important drug discovery in the history of medicine.

What is a legend drug? ›

Legend Drug Definition

A legend drug is a drug approved by the Food and Drug Administration (FDA) for medicinal use if prescribed by a licensed physician or provider. Legend drugs can be both legal and illegal, depending on how they are used. Generally, if it is lawfully prescribed and properly used, it is legal.

Why is Enhertu better than Kadcyla? ›

2021 results from the DESTINY-Breast03 study showed that Enhertu (chemical name: fam-trastuzumab-deruxtecan-nxki) more than doubled the 12-month progression-free survival rate compared to Kadcyla (chemical name: T-DM1 or ado-trastuzumab emtansine) in people diagnosed with metastatic HER2-positive breast cancer that had ...

When did Kadcyla come to market? ›

Based on that trial, the U.S. Food and Drug Administration (FDA) approved marketing on 22 February 2013.
...
Trastuzumab emtansine.
Monoclonal antibody
TypeWhole antibody
SourceHumanized (from mouse)
Clinical data
Trade namesKadcyla
28 more rows

How much trastuzumab is in Kadcyla? ›

Kadcyla 100 mg powder for concentrate for solution for infusion One vial of powder for concentrate for solution for infusion contains 100 mg of trastuzumab emtansine. After reconstitution one vial of 5 mL solution contains 20 mg/mL of trastuzumab emtansine (see section 6.6).

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