I-Mab Past Earnings Performance

Past criteria checks 0/6

I-Mab's earnings have been declining at an average annual rate of -16%, while the Biotechs industry saw earnings growing at 13.4% annually. Revenues have been declining at an average rate of 28.6% per year.

Key information

-16.0%

Earnings growth rate

69.1%

EPS growth rate

Biotechs Industry Growth	-14.6%
Revenue growth rate	-28.6%
Return on equity	-86.9%
Net Margin	-5,887.7%
Last Earnings Update	30 Jun 2024

Recent past performance updates

Recent updates

Revenue & Expenses Breakdown

How I-Mab makes and spends money. Based on latest reported earnings, on an LTM basis.

Earnings and Revenue History

DB:0VY Revenue, expenses and earnings (USD Millions)
Date	Revenue	Earnings	G+A Expenses	R&D Expenses
30 Jun 24	3	-206	63	113
31 Mar 24	4	-205	63	113
31 Dec 23	4	-206	64	114
30 Sep 23	-15	-253	77	117
30 Jun 23	-35	-295	79	124
31 Mar 23	-35	-331	94	131
31 Dec 22	-32	-364	118	131
30 Sep 22	-7	-338	118	139
30 Jun 22	18	-344	127	160
31 Mar 22	17	-365	138	180
31 Dec 21	14	-367	142	191
30 Sep 21	247	-103	118	184
30 Jun 21	242	-4	104	176
31 Mar 21	237	34	82	162
31 Dec 20	236	72	62	151
30 Sep 20	0	-140	56	141
30 Jun 20	2	-171	36	144
31 Mar 20	3	-190	64	131
31 Dec 19	4	-213	94	121
30 Sep 19	6	-172	85	97
30 Jun 19	7	-159	91	71
31 Mar 19	8	-111	51	68
31 Dec 18	8	-59	10	62
31 Dec 17	2	-46	4	41

Quality Earnings: 0VY is currently unprofitable.

Growing Profit Margin: 0VY is currently unprofitable.

Free Cash Flow vs Earnings Analysis

Past Earnings Growth Analysis

Earnings Trend: 0VY is unprofitable, and losses have increased over the past 5 years at a rate of 16% per year.

Accelerating Growth: Unable to compare 0VY's earnings growth over the past year to its 5-year average as it is currently unprofitable

Earnings vs Industry: 0VY is unprofitable, making it difficult to compare its past year earnings growth to the Biotechs industry (-18.6%).

Return on Equity

High ROE: 0VY has a negative Return on Equity (-86.89%), as it is currently unprofitable.

I-Mab Past Earnings Performance

Past criteria checks 0/6

Key information

Recent past performance updates

First half 2024 earnings released: US$0.19 loss per share (vs US$1.32 loss in 1H 2023)

I-Mab to Report First Half, 2024 Results on Aug 28, 2024

Full year 2023 earnings released: CN¥16.53 loss per share (vs CN¥29.23 loss in FY 2022)

I-Mab to Report First Half, 2023 Results on Aug 17, 2023

First half 2022 earnings released: CN¥12.75 loss per share (vs CN¥14.67 loss in 1H 2021)

I-Mab to Report First Half, 2022 Results on Aug 30, 2022

Recent updates

I-Mab Presents Updated Phase 1 Givastomig Data at ESMO 2024

First half 2024 earnings released: US$0.19 loss per share (vs US$1.32 loss in 1H 2023)

I-Mab to Report First Half, 2024 Results on Aug 28, 2024

New minor risk - Market cap size

Insufficient new directors

I-Mab Announces Board and Committee Changes

I-Mab Appoints Phillip Dennis as Chief Medical Officer

I-mab Biopharma (Hangzhou) Co., Ltd. completed the acquisition of I-Mab Biopharma (Shanghai) Co., Ltd. from I-Mab (NasdaqGM:IMAB).

Full year 2023 earnings released: CN¥16.53 loss per share (vs CN¥29.23 loss in FY 2022)

New minor risk - Financial data availability

I-mab Biopharma (Hangzhou) Co., Ltd. agreed to acquire I-Mab Biopharma (Shanghai) Co., Ltd. from I-Mab (NasdaqGM:IMAB) for $80 million.

I-Mab Announces Board Changes , Effective February 10, 2024

I-Mab and Hi-Bio Announces That the U.S. Food and Drug Administration Has Granted Breakthrough Therapy Designation for Felzartamab, an Investigational Cd38 Antibody, for the Treatment of Primary Memorbranous Nephropathy (PMN)

I-Mab Announces Phase 1 Data of Givastomig at Esmo 2023

I-Mab and ABL Bio Announce Latest Updates of PD-L1 and 4-1Bb Bispecific Antibody Tj-L14b Abl503

New major risk - Share price stability

I-Mab (NasdaqGM:IMAB) announces an Equity Buyback for $40 million worth of its shares.

I-Mab to Report First Half, 2023 Results on Aug 17, 2023

I-Mab Announces the Appointment of Raj Kannan as Member of the Board of Directors

TRACON Pharmaceuticals, Inc. Announces Enforcement Action to Collect Binding Arbitration Award from I-Mab Biopharma

First half 2022 earnings released: CN¥12.75 loss per share (vs CN¥14.67 loss in 1H 2021)

Less than half of directors are independent

I-Mab Announces Management Changes

I-Mab Announces Executive Changes

I-Mab(NasdaqGM:IMAB) dropped from FTSE All-World Index (USD)

I-Mab Announces Approval from China CDE to Initiate Phase 3 Registrational Study of Lemzoparlimab in Combination with Azacitidine in Higher-Risk Myelodysplastic Syndrome

I-Mab Announces Positive Phase 2 Data of Lemzoparlimab in Combination with Azacitidine (AZA) in Patients with Higher Risk Myelodysplastic Syndrome at ESMO 2022

I-Mab (NasdaqGM:IMAB) announces an Equity Buyback for $40 million worth of its shares.

I-Mab to Report First Half, 2022 Results on Aug 30, 2022

I-Mab Announces First Patient Dosed in Phase 1 Clinical Trial of Claudin 18.2 and 4-1Bb Bispecific Antibody TJ-CD4B in Solid Tumors in China

Genexine Announces Completion of Enrollment in Phase 3 Clinical Trial with Its Proprietary Long-acting Growth Hormone, GX-H9/TJ101 (Eftansomatropin alfa)

I-Mab Announces Completion of Patient Enrollment in Phase III Clinical Trial of Eftansomatropin Alfa for Treatment of Pediatric Growth Hormone Deficiency

I-Mab Reports Latest Phase 2 Clinical Data of its Differentiated CD73 Antibody Uliledlimab

I-Mab to Hold Investor Call to Report Latest Phase 2 Clinical Data of its Differentiated CD73 Antibody Uliledlimab

I-Mab Reportedly Exploring Possible Sale Amid Takeover Interest

I-Mab Announces First Patient Dosed in China Phase 2 Combination Trial of Lemzoparlimab with Toripalimab in Patients with Advanced Solid Tumors

I-Mab Announces First Patient Dosed in China Phase 2 Clinical Trial of Efineptakin Alfa in Combination with Pembrolizumab in Advanced Solid Tumors

I-Mab Announces IND Approval from China NMPA for Phase 2 Clinical Trial of Enoblituzumab in Combination with Pembrolizumab in Solid Tumors

I-Mab Receives IND Approval for Phase 1 Clinical Trial of Bispecific Antibody TJ-CD4B in Solid Tumors in China

I-Mab Presents Interim Clinical Data of Lemzoparlimab in Combination with Rituximab in Relapsed and Refractory Non-Hodgkin Lymphoma At ASH 2021

I-Mab Announces First Patient Dosed in U.S. Phase 1 Study of Protollin for the Treatment of Alzheimer's Disease

I-Mab Announces First Two Patients Dosed in U.S. Phase 2 Combination Trial of Uliledlimab with Atezolizumab in Patients with Selected Advanced Solid Tumors

I-Mab Announces Acceptance of IND Application from China NMPA for Phase 2 Clinical Trial of Enoblituzumab in Combination with Pembrolizumab in Solid Tumors

Investor sentiment deteriorated over the past week

I-Mab Reports Positive Interim Analysis from Phase 2/3 Study of Its GM-CSF Antibody Plonmarlimab (TJM2) to Treat Patients with Severe Covid-19

Investor sentiment deteriorated over the past week

I-Mab Announces Multiple Advancements of 4-1BB Bispecific Antibody Portfolio

I-Mab Announces China NMPA Approval for Phase 1b Trial of Felzartamab in Systemic Lupus Erythematosus

I-Mab Presents Phase 1 Data on Highly Differentiated CD73 Antibody Uliledlimab at ASCO 2021

I-Mab Announces First Patient Dosed in China Phase 2 Combination Trial of Lemzoparlimab with Azacitidine in Patients with Acute Myeloid Leukemia or Myelodysplastic Syndrome

Investor sentiment improved over the past week

Full year 2020 earnings released: EPS CN¥8.07 (vs CN¥463 loss in FY 2019)

I-Mab Announces Positive Topline Phase 2 Results for Olamkicept in Ulcerative Colitis

Investor sentiment improved over the past week

Full year 2020 earnings released: EPS CN¥8.07 (vs CN¥463 loss in FY 2019)

I-Mab to Present Differentiated Mechanism of Action and Preclinical Data for Anti-CD73 Antibody Uliledlimab At 2021 American Association for Cancer Research Annual Meeting

I-Mab to Report Fiscal Year 2020 Results on Mar 29, 2021

I-Mab Announces First Patient Dosed in China Phase 3 Study of Eftansomatropin Alfa in Pediatric Patients with Growth Hormone Deficiency

I-Mab Announces China NMPA Clearance for Phase 1 Study of TJ210/MOR210 in Patients with Advanced Solid Tumors

I-Mab has completed a Follow-on Equity Offering in the amount of $177.3333 million.

I-Mab Announces Multiple Clinical Advancements of its Differentiated CD73 Antibody Uliledlimab in China and the U.S

I-Mab Announces First Patient Dosed in Phase 2 Clinical Trial of TJ107 in Glioblastoma Multiforme in China

New 90-day high: €51.00

I-Mab and MorphoSys Announce First Patient Dosed in U.S. Phase 1 Study of TJ210/MOR210 in Patients with Advanced Cancer

New 90-day high: €37.60

Revenue in line with expectations

I-Mab Accelerates Clinical Development of Anti-CD47 Monoclonal Antibody Lemzoparlimab in the US and China

Revenue in line with expectations

I-Mab Announces Appointments to its Scientific Advisory Board