Market Cap 58.51B
Revenue (ttm) 29.74B
Net Income (ttm) -1.01B
EPS (ttm) N/A
PE Ratio 10.87
Forward PE 11.76
Profit Margin -3.38%
Debt to Equity Ratio 0.65
Volume 2,150,000
Avg Vol 3,179,216
Day's Range N/A - N/A
Shares Out 3.20B
Stochastic %K 35%
Beta -0.07
Analysts Strong Sell
Price Target $21.97

Company Profile

Takeda Pharmaceutical Company Limited engages in the research, development, manufacture, marketing, and out-licensing of pharmaceutical products. It offers pharmaceutical products in the areas of gastroenterology, rare diseases, plasma-derived therapies, oncology, vaccines, and neuroscience. The company provides its products under the Entyvio, Gattex/Revestive, Takecab/Vocinti, EOHILIA, Takhzyro, Advate, Elaprase, Replagal, Vpriv, Adynovate/Adynovi, Livtencity, ADZYNMA, Gammagard Liquid/Kiovig,...

Industry: Drug Manufacturers - Specialty & Generic
Sector: Healthcare
Phone: 81 3 3278 2111
Address:
1-1, Nihonbashi-Honcho 2-chome, Chuo, Japan
Quantumup
Quantumup Sep. 10 at 1:03 PM
Guggenheim⬆️ $PHVS's PT to $44 from $40, reiterated Buy and said -- CHAPTER-3 delivered injectable-like efficacy—83% & 87% attack reduction overall & in Type 1/2 HAE patients, respectively with the convenience of QD oral medicine. $TAK $BCRX CSLLY IONS KALV - Chiesi Guggenheim added—Pharvaris becomes the one-stop-shop for all things HAE, potentially increasing its strategic optionality. However, two >5x ULN transaminase elevations without bilirubin increases kept a lid on the stock despite stellar efficacy. Company described the LFTs as asymptomatic—one patient discontinued treatment and the other completed the study—with possible contributing factors including, one participant with fatty liver disease, and the other with history of androgen therapy. If these were the only two instances of LFT abnormalities, we don't foresee any labeling or commercial challenges. PT moves to $44 (from $40), which reflects our increased PoS for PHVS-719.
0 · Reply
Quantumup
Quantumup Sep. 9 at 10:23 AM
Citizens⬆️ $PHVS' PT to $79 from $75 and reit'd Outperform $TAK $BCRX CSLLY IONS KALV - Chiesi Wells Fargo⬆️Pharvaris' PT to $65,⬆️PoS to 90% and reit'd Overweight Citizens said in its note: The CHAPTER-3 results are a clear win, with once-daily oral deucrictibant reducing HAE attack rates 83% overall and 87% in Type 1/2 patients, supporting injectable-like efficacy, higher confidence in prophylactic approval and substantial commercial potential, with the April 2027 on-demand PDUFA and subsequent prophylaxis filing/approval as key catalysts. Here's what Wells Fargo said in its note to investors: https://x.com/Quantumup1/status/2097631859517604028?s=20
0 · Reply
Quantumup
Quantumup Sep. 8 at 7:08 PM
Oppenheimer⬆️ $PHVS's PT to $75 and reiterated Outperform after CHAPTER-3 study of deucrictibant XR in HAE prophylaxis met the primary and all secondary endpoints w/ statistical significance. KALV - Chiesi $TAK $BCRX IONS Here's what Oppenheimer said in its note: https://x.com/Quantumup1/status/2097401642534777043?s=20
3 · Reply
Quantumup
Quantumup Sep. 1 at 12:49 PM
Mizuho reiterated $ALKS Outperform-$65 and said -- Given the level of inbound, we consulted with KOLs to gauge their expectations for ALKS-7290 Phase 1b readout in adult ADHD, expected this quarter. $TAK CNTA - $LLY SUPN OTSKY AXSM Here's what else Mizuho had to say: https://x.com/Quantumup1/status/2094769507982024952?s=20
0 · Reply
Quantumup
Quantumup Aug. 31 at 3:23 PM
Wolfe Research reiterated $PTGX Outperform-$225 and said -- "Mimry-Lo And Behold, Another Approval For Protagonist" — ests $2.9B peak sales ($831M in payments to PTGX). $TAK IONS IRON AGIO SLN $JNJ ABBV ALMS ABVX BMY Wolfe Research added—We forecast peak sales of $2.9B in 2036. At this peak (cons $2.6B) and employing the highest 29% royalty rate, PTGX is slated to book $831M in payments. This number assumes just 25% penetration of the PV population. Mgmt. has historically laid out a $1B-$2B peak sales estimate, but we'd caution that this was set before the partners had their hands on the phase 3 data. Indeed, these estimates have not changed since rusfertide subsequently delivered an impressive clinical response in 77% of patients (vs. 33% for placebo).
0 · Reply
DonCorleone77
DonCorleone77 Aug. 31 at 9:58 AM
$PTGX $TAK Protagonist announces Takeda received U.S. FDA approval for MIMRYLO Protagonist Therapeutics (PTGX) announced that Takeda (TAK) received U.S. Food and Drug Administration, FDA, approval for MIMRYLO, a subcutaneously delivered first-in-class hepcidin mimetic peptide for the treatment of erythrocytosis in adults with polycythemia vera. MIMRYLO will be commercialized by Takeda under the worldwide license and collaboration agreement entered into in 2024 between Protagonist and Takeda.
0 · Reply
Cache_Money
Cache_Money Aug. 29 at 2:07 AM
$TAK $PTGX Congratulations Takeda and Protagonist on rusfertide approval. Well deserved!
0 · Reply
StocktwitsNews
StocktwitsNews Aug. 28 at 10:34 PM
NVAX Stock Climbs As Partnership Model Keeps COVID Vaccine Cash Flow Open $NVAX $SNY $TAK https://stocktwits.com/news/equity/markets/nvax-stock-climbs-as-partnership-model-keeps-covid-vaccine-cash-flow-open/cZYAnzkRJrG
0 · Reply
outlawinvestor1
outlawinvestor1 Aug. 28 at 10:15 PM
$PTGX rusfertide approval official - $275M milestone payment triggered. $TAK https://www.fda.gov/news-events/press-announcements/fda-approves-first-drug-its-kind-polycythemia-vera-rare-blood-disorder?utm_medium=email&utm_source=govdelivery
1 · Reply
Quantumup
Quantumup Aug. 27 at 11:11 AM
H.C. Wainwright🏁 $ODTX Buy-$44 and said -- A clinical-stage I&I company built around a potential first-in-class oral RIPK2 scaffolding inhibitor. $TAK $ABVX SYRE ABBV JNJ MRK LLY PFE BMY SNY - TEVA RHHBY Here's what else H.C. Wainwright had to say in its initiation report: https://x.com/Quantumup1/status/2092932646556905587?s=20
0 · Reply
Latest News on TAK
Trump administration to announce drug pricing deals

Mon, 31 Aug 2026 12:09:45 -0400 - 13 days ago

Trump administration to announce drug pricing deals


Takeda receives FDA approval of NDA for Mimrylo

2026-08-28T23:00:13.000Z - 16 days ago

Takeda receives FDA approval of NDA for Mimrylo


Takeda announces Japan MHLW approval for Orzeyful

2026-08-24T09:10:18.000Z - 20 days ago

Takeda announces Japan MHLW approval for Orzeyful


Tuesday's ETF Movers: PPH, PTF

2026-08-18T16:08:58.000Z - 26 days ago

Tuesday's ETF Movers: PPH, PTF


Takeda award from Veterans Affairs posted to SAM.gov site

2026-08-10T12:45:18.000Z - 4 weeks ago

Takeda award from Veterans Affairs posted to SAM.gov site


FDA approves Takeda’s Orzeyful to treat narcolepsy type 1

2026-08-05T22:15:54.000Z - 5 weeks ago

FDA approves Takeda’s Orzeyful to treat narcolepsy type 1


US FDA approves Takeda's sleep disorder pill

Aug 5, 2026, 5:47 PM EDT - 5 weeks ago

US FDA approves Takeda's sleep disorder pill

TAK


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Jul 30, 2026, 6:00 AM EDT - 6 weeks ago

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Takeda Pharmaceutical Company Quarterly report: Q1 2027

Jul 30, 2026, 6:00 AM EDT - 6 weeks ago

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Takeda Pharmaceutical Company Slides: Q1 2027

Jul 30, 2026, 6:00 AM EDT - 6 weeks ago

Takeda Pharmaceutical Company Slides: Q1 2027


Takeda, the Indoensian Government announce collaboration

2026-07-12T23:15:06.000Z - 2 months ago

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Takeda CEO Christophe Weber retires, Julie Kim succeeds

2026-06-24T09:20:15.000Z - 2 months ago

Takeda CEO Christophe Weber retires, Julie Kim succeeds


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Takeda announces results for Phase 3 study of TAK-279


FDA accepts Takeda’s application for intravenous Entyvio

2026-06-09T20:37:00.000Z - 3 months ago

FDA accepts Takeda’s application for intravenous Entyvio


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May 13, 2026, 6:00 AM EDT - 4 months ago

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Takeda Pharmaceutical Company Slides: Q4 2026

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May 13, 2026, 6:00 AM EDT - 4 months ago

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Takeda Pharmaceutical Company Annual report: Q4 2026

May 13, 2026, 6:00 AM EDT - 4 months ago

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Takeda Pharmaceutical Company Transcript: Study Update

Mar 28, 2026, 8:30 PM EDT - 5 months ago

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Takeda Pharmaceutical Company Slides: Study Update

Mar 28, 2026, 8:30 PM EDT - 5 months ago

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Takeda Pharmaceutical Company Earnings Call Transcript: Q3 2026

Jan 29, 2026, 5:30 AM EST - 7 months ago

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Takeda Pharmaceutical Company Quarterly report: Q3 2026

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Takeda Pharmaceutical Company Earnings Call Transcript: Q2 2026

Oct 30, 2025, 6:00 AM EDT - 10 months ago

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Quantumup
Quantumup Sep. 10 at 1:03 PM
Guggenheim⬆️ $PHVS's PT to $44 from $40, reiterated Buy and said -- CHAPTER-3 delivered injectable-like efficacy—83% & 87% attack reduction overall & in Type 1/2 HAE patients, respectively with the convenience of QD oral medicine. $TAK $BCRX CSLLY IONS KALV - Chiesi Guggenheim added—Pharvaris becomes the one-stop-shop for all things HAE, potentially increasing its strategic optionality. However, two >5x ULN transaminase elevations without bilirubin increases kept a lid on the stock despite stellar efficacy. Company described the LFTs as asymptomatic—one patient discontinued treatment and the other completed the study—with possible contributing factors including, one participant with fatty liver disease, and the other with history of androgen therapy. If these were the only two instances of LFT abnormalities, we don't foresee any labeling or commercial challenges. PT moves to $44 (from $40), which reflects our increased PoS for PHVS-719.
0 · Reply
Quantumup
Quantumup Sep. 9 at 10:23 AM
Citizens⬆️ $PHVS' PT to $79 from $75 and reit'd Outperform $TAK $BCRX CSLLY IONS KALV - Chiesi Wells Fargo⬆️Pharvaris' PT to $65,⬆️PoS to 90% and reit'd Overweight Citizens said in its note: The CHAPTER-3 results are a clear win, with once-daily oral deucrictibant reducing HAE attack rates 83% overall and 87% in Type 1/2 patients, supporting injectable-like efficacy, higher confidence in prophylactic approval and substantial commercial potential, with the April 2027 on-demand PDUFA and subsequent prophylaxis filing/approval as key catalysts. Here's what Wells Fargo said in its note to investors: https://x.com/Quantumup1/status/2097631859517604028?s=20
0 · Reply
Quantumup
Quantumup Sep. 8 at 7:08 PM
Oppenheimer⬆️ $PHVS's PT to $75 and reiterated Outperform after CHAPTER-3 study of deucrictibant XR in HAE prophylaxis met the primary and all secondary endpoints w/ statistical significance. KALV - Chiesi $TAK $BCRX IONS Here's what Oppenheimer said in its note: https://x.com/Quantumup1/status/2097401642534777043?s=20
3 · Reply
Quantumup
Quantumup Sep. 1 at 12:49 PM
Mizuho reiterated $ALKS Outperform-$65 and said -- Given the level of inbound, we consulted with KOLs to gauge their expectations for ALKS-7290 Phase 1b readout in adult ADHD, expected this quarter. $TAK CNTA - $LLY SUPN OTSKY AXSM Here's what else Mizuho had to say: https://x.com/Quantumup1/status/2094769507982024952?s=20
0 · Reply
Quantumup
Quantumup Aug. 31 at 3:23 PM
Wolfe Research reiterated $PTGX Outperform-$225 and said -- "Mimry-Lo And Behold, Another Approval For Protagonist" — ests $2.9B peak sales ($831M in payments to PTGX). $TAK IONS IRON AGIO SLN $JNJ ABBV ALMS ABVX BMY Wolfe Research added—We forecast peak sales of $2.9B in 2036. At this peak (cons $2.6B) and employing the highest 29% royalty rate, PTGX is slated to book $831M in payments. This number assumes just 25% penetration of the PV population. Mgmt. has historically laid out a $1B-$2B peak sales estimate, but we'd caution that this was set before the partners had their hands on the phase 3 data. Indeed, these estimates have not changed since rusfertide subsequently delivered an impressive clinical response in 77% of patients (vs. 33% for placebo).
0 · Reply
DonCorleone77
DonCorleone77 Aug. 31 at 9:58 AM
$PTGX $TAK Protagonist announces Takeda received U.S. FDA approval for MIMRYLO Protagonist Therapeutics (PTGX) announced that Takeda (TAK) received U.S. Food and Drug Administration, FDA, approval for MIMRYLO, a subcutaneously delivered first-in-class hepcidin mimetic peptide for the treatment of erythrocytosis in adults with polycythemia vera. MIMRYLO will be commercialized by Takeda under the worldwide license and collaboration agreement entered into in 2024 between Protagonist and Takeda.
0 · Reply
Cache_Money
Cache_Money Aug. 29 at 2:07 AM
$TAK $PTGX Congratulations Takeda and Protagonist on rusfertide approval. Well deserved!
0 · Reply
StocktwitsNews
StocktwitsNews Aug. 28 at 10:34 PM
NVAX Stock Climbs As Partnership Model Keeps COVID Vaccine Cash Flow Open $NVAX $SNY $TAK https://stocktwits.com/news/equity/markets/nvax-stock-climbs-as-partnership-model-keeps-covid-vaccine-cash-flow-open/cZYAnzkRJrG
0 · Reply
outlawinvestor1
outlawinvestor1 Aug. 28 at 10:15 PM
$PTGX rusfertide approval official - $275M milestone payment triggered. $TAK https://www.fda.gov/news-events/press-announcements/fda-approves-first-drug-its-kind-polycythemia-vera-rare-blood-disorder?utm_medium=email&utm_source=govdelivery
1 · Reply
Quantumup
Quantumup Aug. 27 at 11:11 AM
H.C. Wainwright🏁 $ODTX Buy-$44 and said -- A clinical-stage I&I company built around a potential first-in-class oral RIPK2 scaffolding inhibitor. $TAK $ABVX SYRE ABBV JNJ MRK LLY PFE BMY SNY - TEVA RHHBY Here's what else H.C. Wainwright had to say in its initiation report: https://x.com/Quantumup1/status/2092932646556905587?s=20
0 · Reply
WOLFSTREET
WOLFSTREET Aug. 22 at 8:11 PM
$TAK add in divi and round off to 25% gains, i like to diversify! so CC will share all sorts of opps
0 · Reply
jlz1
jlz1 Aug. 19 at 5:56 PM
0 · Reply
EingeLTrade
EingeLTrade Aug. 19 at 5:54 PM
0 · Reply
jlz1
jlz1 Aug. 18 at 2:19 AM
$TAK Should Value Investors Buy Takeda Pharmaceutical Co. (TAK) Stock? https://share.google/iINPUtUnA9xYgP2dA
0 · Reply
jlz1
jlz1 Aug. 13 at 3:06 AM
$TAK rock
0 · Reply
notreload_ai
notreload_ai Aug. 10 at 12:56 PM
$SLN reports 88% response rate for divesiran in polycythemia vera Phase 2 trial. Quarterly dosing could challenge $TAK rusfertide. https://notreload.xyz/xy/silence-divesiran-hits-phase-2-goal-in-rare-blood-cancer/
0 · Reply
nooneknowswhy
nooneknowswhy Aug. 9 at 8:23 PM
0 · Reply
CamilaCruze
CamilaCruze Aug. 8 at 12:45 AM
$TAK Strong pipeline + multiple late-stage programs📈
0 · Reply
handmedown1
handmedown1 Aug. 7 at 2:47 PM
$TAK $CRSP look at tak with approval this v week!!! Lol
0 · Reply
jlz1
jlz1 Aug. 7 at 1:12 PM
$TAK sleep drug approved!!! Easy $25-$30 ?
0 · Reply
NoneNone00
NoneNone00 Aug. 7 at 7:48 AM
$TAK I think LGVN could be the next Sandisk of the biotech world LGVN fully diluted market cap $40 million - $2 billion annual potential revenues (only US and Europe (untapped)) times a p/s of 8 -> $16 billion market cap, for only HLHS (unmet medical need...Hypoplastic Left Heart Syndrome...HLHS phase 2 results August 2026) Extremely promising Alzheimer's results phase 2, in talks for partner for phase 3 green light from FDA to start phase 2 Pediatric Dilated Cardiomyopathy (multi-billion revenue potential) Great results phase 2 Aged related frailty In recent presentation, Longeveron compares itself to stem cell companies, Mesoblast and Capricor both recently valued over $2 billion. I think Longeveron has more potential 50 patents 60 patents pending HLHS program may be eligible for PRV (priority review voucher) upon BLA approval (valued between $150-200 million)
0 · Reply
AvalancheAlpha
AvalancheAlpha Aug. 6 at 5:22 PM
$TAK got FDA approval for a new sleep drug. The market for orexin boosters is real and mostly untapped. But pharma approvals are just the starting line. The hard part is convincing insurers to pay.
0 · Reply